Extended knowledge of 288-42-6

Compound(288-42-6)Formula: C3H3NO received a lot of attention, and I have introduced some compounds in other articles, similar to this compound(Oxazole), if you are interested, you can check out my other related articles.

Epoxy compounds usually have stronger nucleophilic ability, because the alkyl group on the oxygen atom makes the bond angle smaller, which makes the lone pair of electrons react more dissimilarly with the electron-deficient system. Compound: Oxazole, is researched, Molecular C3H3NO, CAS is 288-42-6, about Discovery of Ethyl Ketone-Based Highly Selective HDACs 1, 2, 3 Inhibitors for HIV Latency Reactivation with Minimum Cellular Potency Serum Shift and Reduced hERG Activity.Formula: C3H3NO.

We describe the discovery of histone deacetylase (HDACs) 1, 2, and 3 inhibitors with Et ketone as the zinc-binding group. These HDACs 1, 2, and 3 inhibitors have good enzymic and cellular activity. Their serum shift in cellular potency has been minimized, and selectivity against hERG has been improved. They are also highly selective over HDACs 6 and 8. These inhibitors contain a variety of substituted heterocycles on the imidazole or oxazole scaffold. Compounds 31 and 48 stand out due to their good potency, high selectivity over HDACs 6 and 8, reduced hERG activity, optimized serum shift in cellular potency, and good rat and dog PK profiles.

Compound(288-42-6)Formula: C3H3NO received a lot of attention, and I have introduced some compounds in other articles, similar to this compound(Oxazole), if you are interested, you can check out my other related articles.

Reference:
Oxazolidine – Wikipedia,
Oxazolidine | C3H7NO – PubChem

 

Awesome Chemistry Experiments For 7789-45-9

Here is just a brief introduction to this compound(7789-45-9)Category: oxazolidine, more information about the compound(Cupric bromide) is in the article, you can click the link below.

Category: oxazolidine. So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic. Compound: Cupric bromide, is researched, Molecular Br2Cu, CAS is 7789-45-9, about Tris(3-fluorophenyl)antimony Dihalides: Synthesis and Structure.

Tris(3-fluorophenyl)antimony dichloride, dibromide, and diiodide were obtained by the reaction of tris(3-fluorophenyl)antimony with Cl, Br, and I in benzene. Dichloride and dibromide were also obtained in the reaction of tris(3-fluorophenyl)antimony with Cu dihalides in acetone. Tris(3-fluorophenyl)antimony difluoride was obtained in the exchange reaction between tris(3-fluorophenyl)antimony dichloride and NaF. According to single crystal x-ray diffraction data, centrosym. dichloride and dibromide mols. and four types of crystallog. independent diiodide mols. have a trigonal-bipyramidal configuration with electroneg. ligands in axial positions.

Here is just a brief introduction to this compound(7789-45-9)Category: oxazolidine, more information about the compound(Cupric bromide) is in the article, you can click the link below.

Reference:
Oxazolidine – Wikipedia,
Oxazolidine | C3H7NO – PubChem

 

The origin of a common compound about 5451-40-1

Here is just a brief introduction to this compound(5451-40-1)COA of Formula: C5H2Cl2N4, more information about the compound(2,6-Dichloropurine) is in the article, you can click the link below.

Epoxy compounds usually have stronger nucleophilic ability, because the alkyl group on the oxygen atom makes the bond angle smaller, which makes the lone pair of electrons react more dissimilarly with the electron-deficient system. Compound: 2,6-Dichloropurine, is researched, Molecular C5H2Cl2N4, CAS is 5451-40-1, about Green Regioselective Synthesis of (Purin-6-yl)hydrazones.COA of Formula: C5H2Cl2N4.

Some unique purine hydrazinylidene derivatives I (R1 = Me, CN, CF3; R2 = H, Me, F; R3 = OMe, OEt, pyrazin-2-yl) were synthesized by the regioselective reaction of 2,6-dichloropurine with hydrazine hydrate, followed by condensation with com. available 1,3-dicarbonyl compounds according to a green chem. approach. The regioselectivity of chlorine substitution in 2,6-dichloropurine was established by HMBC (Heteronuclear Multiple Bond Correlation) NMR technique.

Here is just a brief introduction to this compound(5451-40-1)COA of Formula: C5H2Cl2N4, more information about the compound(2,6-Dichloropurine) is in the article, you can click the link below.

Reference:
Oxazolidine – Wikipedia,
Oxazolidine | C3H7NO – PubChem

 

Flexible application of in synthetic route 70-23-5

Here is just a brief introduction to this compound(70-23-5)Recommanded Product: 70-23-5, more information about the compound(Ethyl 3-bromo-2-oxopropanoate) is in the article, you can click the link below.

Recommanded Product: 70-23-5. So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic. Compound: Ethyl 3-bromo-2-oxopropanoate, is researched, Molecular C5H7BrO3, CAS is 70-23-5, about A new “”off-on-off”” sensor for sequential detection of Al3+ and Cu2+ with excellent sensitivity and selectivity based on different sensing mechanisms.

A new simple Schiff base, (E)-N-(2-hydroxybenzylidene)imidazo[2,1-b]thiazole-6-carbohydrazide (X), was designed and synthesized based on salicylaldehyde and imidazo[2, 1-b]thiazole. X could be used as a sensor to identify Al3+ through a significant fluorescence enhancement because of CHEF and inhibition of PET process and then to detect Cu2+ through a highly efficient quenching behavior due to the paramagnetic quenching. The sensor showed a high selectivity for Al3+ and Cu2+ in methanol solution at pH = 5 and was not disturbed by other competing metal ions. Furthermore, based on the equation 3σ/slope, the detection limits of sensor for Al3+ and Cu2+ were calculated to be 3.1 x 10-10 M and 9.8 x 10-11 M, resp. Addnl., the association constants of X[Al3+] and X[Cu2+] were also determined to be 2.3 x 104 M-1 and 6.1 x 104 M-1 on basis of Benesi-Hildebrand equation. In addition, the titration experiment of fluorescence and mass spectrometry showed that sensor was combined with Al3+ or Cu2+ both in 1:1 ratio. Moreover, the optimized structure and energy calculations of X, X[Al3+] and X[Cu2+] were obtained by Gaussian software based on the basis set of B3LYP/6-31 G(d) and B3LYP/LANL2DZ. And, the sensor successfully detected Al3+ and Cu2+ in the real water sample with a satisfactory recovery (91.4 % – 107.1 %) and RSD values (0.66 % – 1.91 %).

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Reference:
Oxazolidine – Wikipedia,
Oxazolidine | C3H7NO – PubChem

 

Now Is The Time For You To Know The Truth About 67914-60-7

Here is just a brief introduction to this compound(67914-60-7)Synthetic Route of C12H16N2O2, more information about the compound(1-(4-(4-Hydroxyphenyl)piperazin-1-yl)ethanone) is in the article, you can click the link below.

Synthetic Route of C12H16N2O2. The protonation of heteroatoms in aromatic heterocycles can be divided into two categories: lone pairs of electrons are in the aromatic ring conjugated system; and lone pairs of electrons do not participate. Compound: 1-(4-(4-Hydroxyphenyl)piperazin-1-yl)ethanone, is researched, Molecular C12H16N2O2, CAS is 67914-60-7, about Synthesis of novel N-9 substituted 6-(4-(4-propoxyphenyl)piperazin-1-yl)-9H-purine derivatives as inducers of apoptosis in MCF-7 breast cancer cells. Author is Sunagar, Manjunath G.; Gaonkar, Supreet; Sunagar, Santosh G.; Deshapande, Narahari; Belavagi, Ningaraddi S.; Khazi, Imtiyaz Ahmed M..

A series of N-9 substituted 6-(4-(4-propoxyphenyl)piperazin-1-yl)-9H-purine derivatives (PP05-PP21) were prepared and evaluated for their anticancer activity against a panel of human cancer cell lines. Evaluation of results revealed that some of the synthesized compounds exhibited promising anticancer activity against the examined cancer cell lines. The structure-activity relationship (SAR) studies in the present work revealed that simple N-9 alkyl substituted 6-(4-(4-propoxyphenyl)piperazin-1-yl)-9H-purines are potent anticancer agents. Among all the compounds, PP17 (9-sec-butyl-6-(4-(4-propoxyphenyl)piperazin-1-yl)-9H-purine) showed good inhibitory activity against MCF-7 cells. Cell cycle anal. of the compound suggested that induces G2/M phase arrest. Biochem. experiments showed that PP17 significantly induced MCF-7 cell apoptosis. Therefore, compound PP17 with a potent in vitro anticancer activity can serve as a promising lead compound for further study.

Here is just a brief introduction to this compound(67914-60-7)Synthetic Route of C12H16N2O2, more information about the compound(1-(4-(4-Hydroxyphenyl)piperazin-1-yl)ethanone) is in the article, you can click the link below.

Reference:
Oxazolidine – Wikipedia,
Oxazolidine | C3H7NO – PubChem

 

The effect of the change of synthetic route on the product 288-42-6

Here is just a brief introduction to this compound(288-42-6)Electric Literature of C3H3NO, more information about the compound(Oxazole) is in the article, you can click the link below.

Electric Literature of C3H3NO. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: Oxazole, is researched, Molecular C3H3NO, CAS is 288-42-6, about Benchmarking doubles-corrected random-phase approximation methods for frequency dependent polarizabilities: Aromatic molecules calculated at the RPA, HRPA, RPA(D), HRPA(D), and SOPPA levels. Author is Joergensen, Maria W.; Sauer, Stephan P. A..

The performance of different polarization propagator methods, such as RPA, RPA(D), HRPA, HRPA(D), and SOPPA, have been tested against CC3 values for both static and dynamic polarizabilities. The test set consists of 14 (hetero-)aromatic medium-sized organic mols., mostly with a high degree of symmetry. The benchmark of the methods remarkably reveals that RPA and HRPA(D) yield results comparable with the CC3 values and that they outperform SOPPA for these mols. For a subset of the mols., a comparison could be made to exptl. values. The comparison for static polarizabilities proves that RPA and HRPA(D) as well as RPA(D) reproduce exptl. values to a satisfying precision, whereas the SOPPA method compared to these three methods appears to perform only adequately. An investigation of the performance of Sadlej’s polarized triple zeta basis set against Dunning’s aug-cc-pVTZ basis set was also carried out. It is found that in contrast to other methods, Sadlej’s basis set did not perform sufficiently compared to the larger aug-cc-pVTZ basis set for the RPA based methods. (c) 2020 American Institute of Physics.

Here is just a brief introduction to this compound(288-42-6)Electric Literature of C3H3NO, more information about the compound(Oxazole) is in the article, you can click the link below.

Reference:
Oxazolidine – Wikipedia,
Oxazolidine | C3H7NO – PubChem

 

Never Underestimate the Influence Of 67914-60-7

Here is just a brief introduction to this compound(67914-60-7)Category: oxazolidine, more information about the compound(1-(4-(4-Hydroxyphenyl)piperazin-1-yl)ethanone) is in the article, you can click the link below.

In general, if the atoms that make up the ring contain heteroatoms, such rings become heterocycles, and organic compounds containing heterocycles are called heterocyclic compounds. An article called Development of Candidates for Positron Emission Tomography (PET) Imaging of Ghrelin Receptor in Disease: Design, Synthesis, and Evaluation of Fluorine-Bearing Quinazolinone Derivatives, published in 2018-02-08, which mentions a compound: 67914-60-7, Name is 1-(4-(4-Hydroxyphenyl)piperazin-1-yl)ethanone, Molecular C12H16N2O2, Category: oxazolidine.

Mol. imaging with positron emission tomog. (PET) is an attractive platform for noninvasive detection and assessment of disease. The development of a PET imaging agent targeting the ghrelin receptor (growth hormone secretagogue receptor type 1a or GHS-R1a) has the potential to lead to the detection and assessment of the higher than normal expression of GHS-R1a in diseases such as prostate, breast, and ovarian cancer. To enable the development of 18F radiopharmaceuticals, we have designed and synthesized three series of quinazolinone derivatives, resulting in the identification of two compound with subnanomolar binding affinity and one fluorine-bearing compound I with picomolar binding affinity (20 pM), representing the highest binding affinity for GHS-R1a reported to date. Two lead compounds (II, IC50 = 20.6 nM; III, IC50 = 9.3 nM) were successfully 18F-radiolabeled with radiochem. purity of greater than 99%. Mol. modeling studies were performed to shed light on ligand-receptor interactions.

Here is just a brief introduction to this compound(67914-60-7)Category: oxazolidine, more information about the compound(1-(4-(4-Hydroxyphenyl)piperazin-1-yl)ethanone) is in the article, you can click the link below.

Reference:
Oxazolidine – Wikipedia,
Oxazolidine | C3H7NO – PubChem

 

Simple exploration of 5451-40-1

In some applications, this compound(5451-40-1)Electric Literature of C5H2Cl2N4 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Electric Literature of C5H2Cl2N4. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: 2,6-Dichloropurine, is researched, Molecular C5H2Cl2N4, CAS is 5451-40-1, about Repurposing Mitsunobu Reactions as a Generic Approach toward Polyethylene Derivatives. Author is Zhang, Yin; Wang, Ting; Bai, Jing; You, Wei.

Broad scope of functionality and controllable degree of functionalization are intriguing goals for the development of polar-group-functionalized polyethylene materials. Herein, we propose a generic strategy of using widely available starting materials (i.e., poly(ethylene-co-vinyl acetate), EVA) and mild Mitsunobu functionalization conditions to prepare over 30 polyethylene derivatives No noble transition metal catalysts (e.g., Ru, Mo, Pd, etc.) or corrosive/explosive reagents (e.g., HBr, NaN3, C2H4, H2, etc.) are used in the synthesis, while functional groups such as azide, aldehyde, norbornene, and thiol can be easily installed, with tunable content as high as 18 mol %. Using this practical method, we successfully prepared polyethylene-derivatized membranes with excellent antimicrobial and fluorescent properties.

In some applications, this compound(5451-40-1)Electric Literature of C5H2Cl2N4 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Reference:
Oxazolidine – Wikipedia,
Oxazolidine | C3H7NO – PubChem

 

An update on the compound challenge: 5451-40-1

In some applications, this compound(5451-40-1)Application In Synthesis of 2,6-Dichloropurine is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

The chemical properties of alicyclic heterocycles are similar to those of the corresponding chain compounds. Compound: 2,6-Dichloropurine, is researched, Molecular C5H2Cl2N4, CAS is 5451-40-1, about Synthesis and photophysical properties of 2-azolyl-6-piperidinylpurines, the main research direction is azolylpiperidinylpurine preparation fluorescence MSPR.Application In Synthesis of 2,6-Dichloropurine.

A synthesis of fluorescent 2-azolyl-6-piperidinylpurines was designed. Azolyl substituent at purine C-2 atom was introduced via nucleophilic aromatic substitution or in the case of tetrazolyl and 1,2,3-triazolyl substituents via a ring formation on a preinstalled amine or azide moiety, resp. The obtained purine intermediates were functionalized at N-9 position using Mitsunobu reaction conditions and achieved amorphous compounds, which formed a thin-layer films of good quality. The push-pull systems exhibited fluorescence with emission in range of 360-400 nm and quantum yields up to 66% in CH2Cl2 solution and up to 45% in the thin-layer film.

In some applications, this compound(5451-40-1)Application In Synthesis of 2,6-Dichloropurine is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Reference:
Oxazolidine – Wikipedia,
Oxazolidine | C3H7NO – PubChem

 

Awesome and Easy Science Experiments about 70-23-5

In some applications, this compound(70-23-5)Application of 70-23-5 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called ZnO-nanocatalyst Promoted the Production of Imidazole Derivatives via four-component Reaction of Amino acid: Study of Antioxidant and Antimicrobial Activity, published in 2021-07-31, which mentions a compound: 70-23-5, mainly applied to zinc oxide nanocatalyst imidazole derivative production antioxidant antimicrobial activity; Alkyl bromides; aminoacides; catalyst; imidazole; multicomponent reactions; zinc oxide nanoparticles (ZnO-NPs), Application of 70-23-5.

In current research, imidazole derivatives are synthesized via a new process of four component reaction of trichloroacetonitrile, amides, alkyl bromides and amino acids catalyzed by zinc oxide nanoparticles (ZnO-NPs) as a simple and recyclable catalyst in water at room temperature Among investigated compounds, compounds 5b have good results relative to butylated hydroxytoluene (BHT) and 2-tert-butylhydroquinone (TBHQ) as standard antioxidant. The achieved outcomes of disk diffusion experiment showed that these compounds avoided the growth of bacterial. In this research, all chems. are purchased from Fluka (Buchs, Switzerland) and employed with any purification For measuring IR spectroscopy and m.p., a Shimadzu IR-460 spectrometer and Electrothermal 9100 apparatus are utilized resp. BRUKER DRX-400 AVANCE spectrometer is used for giving the 1H, and 13CNMR spectra at 400.1 and 100 MHz resp. For recording mass spectra, a FINNIGAN-MAT 8430 spectrometer with an ionization potential of 70 eV was utilized. The SEM employing a Holland Philips XL30 microscope was used for determination of ZnO nanocomposites morphol. X-ray diffraction anal. at room temperature using a Holland Philips Xpert X-ray powder diffractometer, with CuKα radiation (λ=0.15406 nm), with 2θ ranging from 20 to 80° was employed for characterization of crystalline structure of Fe3O4/CuO nanocomposites. Scherrer’s formula; D= 0.9λ/β cosθ was employed for calculating the average crystallite size where D is the diameter of the nanoparticles, λ (CuKα) =1.5406 Å and β is the full width at half-maximum of the diffraction lines. A general way to prepare of compounds 5 The trichloroacetonitrile 1 (2 mmol) and amides 2 (2 mmol) mixed with ZnO-NPs (10 mol%) in water (5 mL). after 45 min amino acids 3 (2 mmol) was added to previous mixture at room temperature After 30 min α-haloketones 4 (2 mmol) was added to mixture and stirred for 3 h. After 3 h, the reaction is completed and TLC confirms progress of the reaction. At last, the solid residue was collected by filtration and cleaned with EtOAC to removing ZnO-NPs and after evaporating solvent and washing solid with Et2O compounds 5 afforded as pure product. Without employing catalyst, these reactions have low yield and busy mixture The synthesis of compound 5a as sample reaction and displayed the ZnO nanoparticles (10 mol%) is the best catalyst for sample reaction and H2O is the very better than other solvent in sample reaction. Structures of 5 are confirmed by IR, 1H NMR, 13C NMR mass spectra. In summary, imidazole derivatives were produced in excellent yield from the reaction of trichloroacetonitrile, amides, alkyl bromides and amino acids using ZnO-NPs in water at room temperature In addition, the power of synthesized imidazole as antioxidant was determined by radical trapping of DPPH and power of reducing ferric analyzes. The tested imidazoles display good radical trapping of DPPH but exhibitted moderate FRAP relative to BHT and TBHQ as synthetic antioxidants. The outcomes of disk diffusion experiment exhibits that synthesized imidazole avoided the bacterial growth. The superiorities of this procedure are environmental, high yield of product and low amounts of catalyst and short time of reaction.

In some applications, this compound(70-23-5)Application of 70-23-5 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Reference:
Oxazolidine – Wikipedia,
Oxazolidine | C3H7NO – PubChem