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Ethyl 5-chloro-1,3,4-thiadiazole-2-carboxylate is a chemical compound characterized by the molecular formula C6H6ClN3O2S. It is a thiadiazole derivative, a five-membered heterocyclic ring with three nitrogen atoms, one sulfur atom, and one carbon atom. As an ester, it features the functional group COOattached to the thiadiazole ring. The chlorine atom and carboxylate group contribute to its utility in synthetic organic chemistry, making it a valuable building block for the development of more complex molecules. Its unique properties and potential applications in pharmaceuticals, agrochemicals, and materials science have garnered attention from researchers and chemists.

64837-49-6

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64837-49-6 Usage

Uses

Used in Pharmaceutical Industry:
Ethyl 5-chloro-1,3,4-thiadiazole-2-carboxylate is used as a synthetic intermediate for the development of pharmaceutical compounds. Its unique structure and functional groups enable the creation of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, Ethyl 5-chloro-1,3,4-thiadiazole-2-carboxylate serves as a key building block for the synthesis of agrochemicals, such as pesticides and herbicides. Its properties allow for the development of effective and targeted agricultural products.
Used in Materials Science:
Ethyl 5-chloro-1,3,4-thiadiazole-2-carboxylate is utilized in materials science for the synthesis of novel materials with specific properties. Its incorporation into polymers and other materials can lead to advancements in areas such as electronics, coatings, and adhesives.
Used in Organic Synthesis:
As a versatile building block in organic synthesis, Ethyl 5-chloro-1,3,4-thiadiazole-2-carboxylate is employed in the preparation of various organic compounds. Its reactivity and functional groups make it a valuable component in the synthesis of complex molecules for research and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 64837-49-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,8,3 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 64837-49:
(7*6)+(6*4)+(5*8)+(4*3)+(3*7)+(2*4)+(1*9)=156
156 % 10 = 6
So 64837-49-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H5ClN2O2S/c1-2-10-4(9)3-7-8-5(6)11-3/h2H2,1H3

64837-49-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 5-chloro-1,3,4-thiadiazole-2-carboxylate

1.2 Other means of identification

Product number -
Other names 1,3,4-Thiadiazole-2-carboxylic acid,5-chloro-,ethyl ester

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:64837-49-6 SDS

64837-49-6Relevant academic research and scientific papers

Aryl hetero ring-substituted aromatic compound (by machine translation)

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Paragraph 0225-0226, (2020/09/17)

[Problem] β - lactamase inhibiting action in a new compound. (1A) or (1b) or a compound represented by the formula [a] to pharmaceutically acceptable salts. [(1A) (1b) and in the formula, g is, O, etc. S; X is, a hydroxyl group, an alkoxy group such as C1

COMPOUNDS THAT MODULATE EGFR ACTIVITY AND METHODS FOR TREATING OR PREVENTING CONDITIONS THEREWITH

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Page/Page column 96, (2011/07/09)

Provided are compounds and methods for treating or preventing kinase-mediated disorders therewith.

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