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2055-52-9

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2055-52-9 Usage

Methyl ester derivative

1-Phenyl-1H-[1,2,3]triazole-4-carboxylic acid The compound is derived from 1-phenyl-1H-[1,2,3]triazole-4-carboxylic acid by attaching a methyl ester group.

Five-membered heterocyclic compound

1,2,3-triazole The core structure of this compound is a five-membered ring containing three nitrogen atoms and two carbon atoms.

Importance in synthesis

Pharmaceuticals, agrochemicals, and materials Triazoles and their derivatives, including this compound, are valuable building blocks in the synthesis of various products.

Potential applications

Synthetic intermediate, pharmaceutical research and development The compound may be used as a synthetic intermediate in organic chemistry or in pharmaceutical research and development.

Specific properties and applications

Dependent on further research and testing The exact properties and potential applications of this compound would need to be determined through additional studies and experiments.

Check Digit Verification of cas no

The CAS Registry Mumber 2055-52-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,5 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2055-52:
(6*2)+(5*0)+(4*5)+(3*5)+(2*5)+(1*2)=59
59 % 10 = 9
So 2055-52-9 is a valid CAS Registry Number.

2055-52-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Phenyl-1H-[1,2,3]triazole-4-carboxylic acid methyl ester

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2055-52-9 SDS

2055-52-9Relevant articles and documents

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)

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

Design, synthesis and antibacterial evaluation of novel 15-membered 11a-azahomoclarithromycin derivatives with the 1, 2, 3-triazole side chain

Qin, Yinhui,Teng, Yuetai,Ma, Ruixin,Bi, Fangchao,Liu, Zhiyang,Zhang, Panpan,Ma, Shutao

, p. 321 - 339 (2019/07/18)

Macrolides are widely prescribed in clinic to treat various respiratory tract infections. However, due to their inappropriate use, the prevalence of macrolide-resistant strains among clinical isolates has become a concern for public health. Therefore, nov

Catalytic Intermolecular Cross-Couplings of Azides and LUMO-Activated Unsaturated Acyl Azoliums

Li, Wenjun,Ajitha, Manjaly J.,Lang, Ming,Huang, Kuo-Wei,Wang, Jian

, p. 2139 - 2144 (2017/08/14)

An example for the catalytic synthesis of densely functionalized 1,2,3-triazoles through a LUMO activation mode has been developed. The protocol is enabled by intermolecular cross-coupling reactions of azides with in situ-generated α,β-unsaturated acyl az

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