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Methyl 1-phenyl-1H-1,2,3-triazole-5-carboxylate is a chemical compound with the molecular formula C10H8N2O2. It is a derivative of 1,2,3-triazole, a heterocyclic organic compound consisting of a five-membered ring with three nitrogen atoms and two carbon atoms. This specific compound features a phenyl group attached to the triazole ring and a carboxylate group at the 5-position, with a methyl group esterifying the carboxylate. Methyl 1-phenyl-1H-1,2,3-triazole-5-carboxylate is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of fungicides. Its chemical structure and properties make it a versatile building block in organic synthesis, allowing for the creation of a wide range of compounds with potential applications in different industries.

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  • 5315-72-0 Structure
  • Basic information

    1. Product Name: methyl 1-phenyl-1H-1,2,3-triazole-5-carboxylate
    2. Synonyms: methyl 1-phenyl-1H-1,2,3-triazole-5-carboxylate
    3. CAS NO:5315-72-0
    4. Molecular Formula:
    5. Molecular Weight: 203.2
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 5315-72-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: methyl 1-phenyl-1H-1,2,3-triazole-5-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 1-phenyl-1H-1,2,3-triazole-5-carboxylate(5315-72-0)
    11. EPA Substance Registry System: methyl 1-phenyl-1H-1,2,3-triazole-5-carboxylate(5315-72-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 5315-72-0(Hazardous Substances Data)

5315-72-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5315-72-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,1 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5315-72:
(6*5)+(5*3)+(4*1)+(3*5)+(2*7)+(1*2)=80
80 % 10 = 0
So 5315-72-0 is a valid CAS Registry Number.

5315-72-0Relevant articles and documents

Unveiling Potent Photooxidation Behavior of Catalytic Photoreductants

Targos, Karina,Williams, Oliver P.,Wickens, Zachary K.

, p. 4125 - 4132 (2021)

We describe a photocatalytic system that reveals latent photooxidant behavior from one of the most reducing conventional photoredox catalysts, N-phenylphenothiazine (PTH). This aerobic photochemical reaction engages difficult to oxidize feedstocks, such as benzene, in C(sp2)-N coupling reactions through direct oxidation. Mechanistic studies are consistent with activation of PTH via photooxidation and with Lewis acid cocatalysts scavenging inhibitors inextricably formed in this process.

The azide-alkyne cycloaddition catalysed by transition metal oxide nanoparticles

Molteni, Giorgio,Ferretti, Anna M.,Trioni, Mario Italo,Cargnoni, Fausto,Ponti, Alessandro

, p. 18049 - 18061 (2019/12/03)

Colloidal nanoparticles of Earth-abundant, first-row transition metal oxides and sulfide, namely magnetite (Fe3O4), manganese and cobalt ferrite, (MnFe2O4, CoFe2O4), manganese(ii) oxide (Mn

TBAI or KI-Promoted Oxidative Coupling of Enamines and N-Tosylhydrazine: An Unconventional Method toward 1,5- and 1,4,5-Substituted 1,2,3-Triazoles

Huang, Wei,Zhu, Chuanle,Li, Minke,Yu, Yue,Wu, Wanqing,Tu, Zhengchao,Jiang, Huanfeng

, p. 3117 - 3123 (2018/08/01)

A novel method for the synthesis of 1,5- and 1,4,5-substituted 1,2,3-triazoles has been reported. This approach is promoted by iodine-TBHP oxidation system using enamines and N-tosylhydrazine as materials, which avoid the dependence of traditional methods on azides and transition metals. Through this approach, various 1,5- and 1,4,5-substituted 1,2,3-triazoles were delivered in moderate to high yields. The mechanistic study indicated that an amino exchange would be involved in the reaction process. Moreover, the product methyl 1-(2-methoxyphenyl)-4-methyl-1H-1,2,3-triazole-5-carboxylate is a useful precursor to anti-influenza A agent, and further application research was conducted. (Figure presented.).

Pressure-accelerated azide-alkyne cycloaddition: Micro capillary versus autoclave reactor performance

Borukhova, Svetlana,Seeger, Andreas D.,Nol, Timothy,Wang, Qi,Busch, Markus,Hessel, Volker

, p. 504 - 512 (2015/03/04)

Pressure effects on regioselectivity and yield of cycloaddition reactions have been shown to exist. Nevertheless, high pressure synthetic applications with subsequent benefits in the production of natural products are limited by the general availability o

3-nitro- and 3-bromo-3-nitroacrylates in reactions with phenyl azide

Berestovitskaya,Anisimova,Kataeva,Makarova,Berkova

, p. 1567 - 1575 (2008/03/14)

1,3-Dipolar cycloaddition of alkyl 3-nitro-and 3-bromo-3-nitroacrylates to phenyl azide gives regioisomeric alkyl 5(4)-nitro-1-phenyl-4,5-dihydro-1H-1,2,3- triazole-4(5)-carboxylates, the corresponding triazoles both with and without nitro group, and alky

Arylazide cycloaddition to methyl propiolate: DFT-based quantitative prediction of regioselectivity

Molteni, Giorgio,Ponti, Alessandro

, p. 2770 - 2774 (2007/10/03)

Several 1-(4-substituted)-phenyl-4- or 5-methoxycarbonyl-1,2,3-triazoles have been synthesized by 1,3-dipolar cycloaddition of the corresponding arylazides to methyl propiolate in carbon tetrachloride. The regioselectivity of these reactions cannot be rat

CYCLOADDITION DES METHYLAZIDE ET PHENYLAZIDE AU β-NITROSTYRENE ET AU NITROPROPENE HOMOLOGUE

Cailleux, P.,Piet, J. C.,Benhaoua, H.,Carrie, R.

, p. 45 - 52 (2007/10/03)

Phenylazide and methylazide reacts with title olefines and gives two isomeric triazoles without nitro group, and 4-nitro-1,2,3 triazole.The isomerisation of starting alkenes explains the formation of isomeric triazoles.Oxydation of amino-nitro-diazocompounds in equilibrium with 1,2,3 triazolines leads to 4-nitro-1,2,3 triazoles.

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