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1H-1,2,3-Triazole-5-carboxylicacid,1-ethyl-,methylester(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

215872-74-5

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215872-74-5 Usage

Derivative of 1,2,3-triazole

five-membered ring compound
1,2,3-Triazole is a five-membered ring compound containing three nitrogen atoms and two carbon atoms.

Methyl ester

methoxy group attached to carboxylic acid functional group
A methyl ester is formed when a methoxy group (-OCH3) is attached to the carboxylic acid (-COOH) functional group.

1-ethyl derivative

ethyl group attached to the triazole ring
An ethyl group (-CH2CH3) is attached to the triazole ring, making it a 1-ethyl derivative.

Applications

organic synthesis, pharmaceuticals, and materials science
Due to the unique properties and reactivity of the triazole ring, 1H-1,2,3-Triazole-5-carboxylicacid,1-ethyl-,methylester(9CI) may have applications in various fields.

Potential pharmaceutical applications

structural similarity to existing drugs and bioactive molecules
The compound may have potential pharmaceutical applications due to its structural similarity to other drugs and bioactive molecules containing the triazole ring.

Chemical structure

contains a triazole ring, an ester group, and an ethyl group
The chemical structure of 1H-1,2,3-Triazole-5-carboxylicacid,1-ethyl-,methylester(9CI) consists of a triazole ring, an ester group (formed by the attachment of a methoxy group to the carboxylic acid), and an ethyl group attached to the triazole ring.

Functional groups

triazole, carboxylic acid, ester, and alkyl (ethyl) groups
The compound contains several functional groups, including a triazole ring, a carboxylic acid, an ester group, and an alkyl (ethyl) group.

Reactivity

may undergo various chemical reactions due to its functional groups
The presence of multiple functional groups in the molecule allows for a range of chemical reactions, such as esterification, substitution, and addition reactions.

Solubility

may be soluble in organic solvents
Due to the presence of the ester and alkyl groups, 1H-1,2,3-Triazole-5-carboxylicacid,1-ethyl-,methylester(9CI) may be soluble in organic solvents like ethanol, methanol, or acetone.

Check Digit Verification of cas no

The CAS Registry Mumber 215872-74-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,5,8,7 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 215872-74:
(8*2)+(7*1)+(6*5)+(5*8)+(4*7)+(3*2)+(2*7)+(1*4)=145
145 % 10 = 5
So 215872-74-5 is a valid CAS Registry Number.

215872-74-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-ethyltriazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names methyl 1-ethyl-1,2,3-triazole-5-carboxylate

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:215872-74-5 SDS

215872-74-5Downstream Products

215872-74-5Relevant academic research and scientific papers

ZnO nanoparticles-mediated regioselective synthesis of methyl-iV-alkylated 1,2,3-triazole-4-carboxylates

Prabakaran,Khan, Fazlur-Rahman Nawaz,Jin, Jong Sung

experimental part, p. 1101 - 1109 (2012/08/28)

The 1,2,3-triazoles are versatile synthetic intermediates of many biologically active compounds, and their N-1 substituted analogues are potential pharmaceutically important derivatives. In this study, an efficient regioselective N-alkylation reaction of

NOVEL HERBICIDES

-

Page/Page column 111, (2008/06/13)

Compounds of formula I: wherein R1, R2, R3, R4, m, R5, R6, n and Y are as defined in claim 1; or N-oxides, salts and optical isomers thereof. Furthermore, the present invention relates to processes for preparing compounds of formula (I), to herbicidal compositions comprising them and to methods of using them to control plants or to inhibit plant growth.

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