A new synthetic route of 1194-22-5

Compound(1194-22-5)HPLC of Formula: 1194-22-5 received a lot of attention, and I have introduced some compounds in other articles, similar to this compound(6-Hydroxy-2-methylpyrimidin-4(3H)-one), if you are interested, you can check out my other related articles.

Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, International Annual Conference of ICT called Calorimetric and theoretical investigation of heat effects and reaction kinetics for nitration of 2-methyl-4,6-dihydroxy-pyrimidine, Author is Chylek, Zbigniew; Trzcinski, Waldemar A., which mentions a compound: 1194-22-5, SMILESS is CC1=NC(=CC(N1)=O)O, Molecular C5H6N2O2, HPLC of Formula: 1194-22-5.

The thermal effects accompanying the process of nitration of 2-methyl-4,6-dihydroxy-pyrimidine (other names in use: 2-methylpyrimidine-4,6-dione, MPD) were investigated. Measurements were performed using a differential reaction calorimeter (DRC). The heat of solution of MPD in concentrated sulfuric acid (95%), the heat of mixing of nitric acid (100%) with sulfuric acid (95%) and the heat effect of nitration of MDP in a mixture of nitric and sulfuric acids were measured. Anal. of literature data and the research results allowed to propose the model and math. formulation of the problem of the nitration of MPD. The model was used to simulate phenomena and reactions running in DRC. The exptl. data were compared with modeling results. The parameters of the rate constants of reactions running in DRC were determined

Compound(1194-22-5)HPLC of Formula: 1194-22-5 received a lot of attention, and I have introduced some compounds in other articles, similar to this compound(6-Hydroxy-2-methylpyrimidin-4(3H)-one), if you are interested, you can check out my other related articles.

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 %).

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.

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

 

Why do aromatic interactions matter of compound: 1194-22-5

In some applications, this compound(1194-22-5)Category: oxazolidine is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 1194-22-5, is researched, SMILESS is CC1=NC(=CC(N1)=O)O, Molecular C5H6N2O2Conference, New Trends in Research of Energetic Materials, Proceedings of the Seminar, 10th, Pardubice, Czech Republic, Apr. 25-27, 2007 called On the synthesis of 1,1-diamino-2,2-dinitroethene (FOX-7) by nitration of 4,6-dihydroxy-2-methylpyrimidine, Author is Johansson, Martin; Latypov, Nikolaj V.; Holmgren, Erik; Sizova, Ekaterina V.; Sizov, Vladimir; Bellamny, Anthony J., the main research direction is dihydroxy methylpyrimidine nitration diamino dinitroethene explosive.Category: oxazolidine.

The synthesis of 1,1-diamino-2,2-dinitroethene (FOX-7) by nitration of 4, 6-dihydroxy-2-methylpyrimidine and hydrolysis of the resulting intermediate 2-dinitromethylene-5,5-dinitropyrimidine-4, 6-dione has been studied. By varying the reactions parameters the optimal conditions for the synthesis of FOX-7 have been identified and gave a >90% yield of the pure product. The optimized process allowed the spent acid to be recycled without loss of yield, with almost stoichiometric consumption of nitric acid. The purity of the FOX-7 has been determined using a newly developed HPLC method.

In some applications, this compound(1194-22-5)Category: oxazolidine 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

 

Why do aromatic interactions matter of compound: 1194-22-5

In some applications, this compound(1194-22-5)Reference of 6-Hydroxy-2-methylpyrimidin-4(3H)-one 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 The effect of some derivatives of pyrimidine on metastasis of the transplantable rat sarcoma SSK, published in 1963, which mentions a compound: 1194-22-5, mainly applied to , Reference of 6-Hydroxy-2-methylpyrimidin-4(3H)-one.

Sarcoma SSK was transferred to normal rats by injection of a tumor cell suspension in physiol. saline containing penicillin into the middle third of the tail. Treatment by intraperitoneal injection of metacil (I), 2-methyl-4,6-dioxypyrimidine (II), thymine (III), dihydrothymine (IV), cytosine (V), isocytosine (VI), 4,6-dioxy-5-nitropyrimidine (VII), 2,6-mercapto-5-amino-4-methylpyrimidine (VIII), and pentoxyl (IX) in solution or suspension in physiol. saline in doses of 100 mg./kg./day was begun within 24 hrs., and continued for 19 days. Control animals received physiol. saline. In one group, the tails were amputated after 5 days; in the second, after 9 days. In the 1st group, animals which received VII all died in the postoperative period, while those which received I, II, V, VI, or IX developed fewer metastases than the controls. No such inhibitory effect of metastasis was observed in the 2nd group. In both groups, animals which received III, IV, or VIII developed more metastases than the controls.

In some applications, this compound(1194-22-5)Reference of 6-Hydroxy-2-methylpyrimidin-4(3H)-one 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

 

Simple exploration of 70-23-5

In some applications, this compound(70-23-5)SDS of cas: 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.

Srinivasarao, Talasila; Mohanty, Sandeep; Venkata, Suryanarayana C. H.; Reddy, G. Sandeep; Jaydeepkumar; Rao, B. Venkateswara published the article 《An efficient and novel process for the synthesis of nizatidine》. Keywords: dimethylamino ethanethioamide ethyl bromopyruvate green cyclocondensation reduction amination; nizatidine preparation.They researched the compound: Ethyl 3-bromo-2-oxopropanoate( cas:70-23-5 ).SDS of cas: 70-23-5. Aromatic heterocyclic compounds can be divided into two categories: single heterocyclic and fused heterocyclic. In addition, there is a lot of other information about this compound (cas:70-23-5) here.

A facile eco-friendly, cost effective and robust process for the synthesis of Nizatidine via the cyclocondensation of 2-(dimethylamino)ethanethioamide with Et bromopyruvate followed by reduction then coupled with cysteamine hydrochloride. The later formed product was coupled with N-methyl-1-(methylthio)-2-nitroethenamine in water resulted Nizatidine. The synthesized product met European pharmacopeia (EP) monograph.

In some applications, this compound(70-23-5)SDS of cas: 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

 

New learning discoveries about 5451-40-1

When you point to this article, it is believed that you are also very interested in this compound(5451-40-1)Formula: C5H2Cl2N4 and due to space limitations, I can only present the most important information.

Heterocyclic compounds can be divided into two categories: alicyclic heterocycles and aromatic heterocycles. Compounds whose heterocycles in the molecular skeleton cannot reflect aromaticity are called alicyclic heterocyclic compounds. Compound: 5451-40-1, is researched, Molecular C5H2Cl2N4, about 1,2,3-Triazoles as leaving groups in SNAr-arbuzov reactions: synthesis of C6-phosphonated purine derivatives, the main research direction is heptyl bisphenyltriazolyl purine regioselective nucleophilic aromatic substitution Arbuzov reaction; diethoxyphosphoryl heptyl triazolyl purine preparation; 2,6-bistriazolylpurines; Arbuzov reaction; nucleophilic aromatic substitution; purinylphosphonates.Formula: C5H2Cl2N4.

A new method for C-N bond transformations into C-P bonds was developed using 1,2,3-triazoles as leaving groups in SNAr-Arbuzov reactions. A series of C6-phosphonated 2-triazolylpurine derivatives I [R = methoxycarbnonyl, Bu, 2-pyridyl, etc.] was synthesized for the first time, with the isolated yields reaching up to 82% in the C-P-bond-forming event. The SNAr-Arbuzov reaction of 2,6-bistriazolylpurines follows the general regioselectivity pattern of the C6-position being more reactive towards substitution, which was unambiguously proved by X-ray anal. of I [R = phenyl].

When you point to this article, it is believed that you are also very interested in this compound(5451-40-1)Formula: C5H2Cl2N4 and due to space limitations, I can only present the most important information.

Reference:
Oxazolidine – Wikipedia,
Oxazolidine | C3H7NO – PubChem