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ETHYL 5-METHYL-2H-1,2,4-TRIAZOLE-3-CARBOXYLATE is an organic compound with the molecular formula C6H8N2O2. It is a derivative of 1,2,4-triazole, a five-membered ring containing three nitrogen atoms. ETHYL 5-METHYL-2H-1,2,4-TRIAZOLE-3-CARBOXYLATE is characterized by its potential applications in the synthesis of various chemical compounds and its role in the development of therapeutic agents.

40253-47-2

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40253-47-2 Usage

Uses

Used in Pharmaceutical Industry:
ETHYL 5-METHYL-2H-1,2,4-TRIAZOLE-3-CARBOXYLATE is used as a reagent for the synthesis of low-molecular derivatives of 1,2,4-triazole. These derivatives have potential applications in the development of pharmaceutical compounds due to their diverse chemical properties and reactivity.
Used in Cancer Treatment and Hypoxia Mediated Disease Industry:
ETHYL 5-METHYL-2H-1,2,4-TRIAZOLE-3-CARBOXYLATE is used as a reagent in the preparation of heterocyclic modulators of HIF (Hypoxia-Inducible Factor) activity. HIF is a transcription factor that plays a crucial role in the cellular response to low oxygen levels (hypoxia) and is often overexpressed in various cancers and other hypoxia-mediated diseases. By modulating HIF activity, these heterocyclic modulators can potentially be used in the treatment of cancer and other hypoxia-mediated diseases, offering a novel therapeutic approach to these conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 40253-47-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,2,5 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 40253-47:
(7*4)+(6*0)+(5*2)+(4*5)+(3*3)+(2*4)+(1*7)=82
82 % 10 = 2
So 40253-47-2 is a valid CAS Registry Number.

40253-47-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 5-methyl-1H-1,2,4-triazole-3-carboxylate

1.2 Other means of identification

Product number -
Other names Ethyl 5-methyl-4H-1,2,4-triazole-3-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:40253-47-2 SDS

40253-47-2Relevant academic research and scientific papers

An Efficient Route to Ethyl 5-Alkyl- (Aryl)-1H-1,2,4-triazole-3-carboxylates

Chudinov,Matveev,Zhurilo,Prutkov,Shvets

, p. 1273 - 1277 (2015)

An efficient general route to the synthesis of 5-substituted 1H-1,2,4-triazole-3-carboxylates was developed. N-acylamidrazones were obtained from carboxylic acid hydrazides and ethyl thiooxamate or ethyl 2-ethoxy-2-iminoacetate hydrochloride and then were

PREPARATION OF 3- AND 3,5-SUBSTITUTED 1,2,4-TRIAZOLES

Vanek, Tomas,Velkova, Vlasta,Gut, Jiri

, p. 2492 - 2495 (2007/10/02)

Ethyl 1,2,4-triazole-3-carboxylate (V), its 5-methyl and 5-phenyl derivatives (V and VI, respectively), 3-methyl-1,2,4-triazole (VIII), 3-phenyl-1,2,4-triazole (IX), 3,5-dimethyl-1,2,4-triazole (X), 3,5-diphenyl-1,2,4-triazole (XI) and 3-phenyl-5-methyl-1,2,4-triazole (XII) were prepared in 40-70percent yields by thermal cyclization of acylamidrazones III.

HETEROCYCLIC SYNTHESIS USING ETHYL CARBOETHOXYFORMIMIDATE

McKillop, Alexander,Henderson, Alan,Ray, Partha S.,Avendano, Carmen,Molinero, Encarnacion G.

, p. 3357 - 3360 (2007/10/02)

Ethyl carboethoxyformimidate is shown to be a versatile reagent for the synthesis of a variety of mono- and bicyclic heterocyclic systems.

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