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2-Chlorothiazole-5-sulfonyl chloride is a chemical compound with the molecular formula C4H3ClN2O2S2. It is a sulfonyl chloride derivative of 2-chlorothiazole, characterized by its clear, colorless to slightly yellow liquid appearance and a pungent odor. This highly reactive compound is known for its reactivity towards nucleophiles, making it a valuable reagent in organic synthesis for introducing the sulfonyl chloride functional group into various organic compounds.

88917-11-7

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88917-11-7 Usage

Uses

Used in Pharmaceutical Industry:
2-Chlorothiazole-5-sulfonyl chloride is used as a key intermediate in the synthesis of thiazole-based pharmaceuticals and agrochemicals. Its ability to introduce the sulfonyl chloride group aids in the development of new therapeutic agents and pesticides.
Used in Production of Dyes and Fine Chemicals:
In the chemical industry, 2-Chlorothiazole-5-sulfonyl chloride is utilized for the production of dyes and other fine chemicals, where its reactivity is harnessed to create a variety of specialty compounds.
Safety Considerations:
It is crucial to handle 2-chlorothiazole-5-sulfonyl chloride with care due to its classification as a hazardous material. Exposure can result in skin, eye, and respiratory system irritation, necessitating proper safety measures during its use and storage.

Check Digit Verification of cas no

The CAS Registry Mumber 88917-11-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,9,1 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 88917-11:
(7*8)+(6*8)+(5*9)+(4*1)+(3*7)+(2*1)+(1*1)=177
177 % 10 = 7
So 88917-11-7 is a valid CAS Registry Number.

88917-11-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chlorothiazole-5-sulfonyl chloride

1.2 Other means of identification

Product number -
Other names 2-chloro-1,3-thiazole-5-sulfonyl chloride

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:88917-11-7 SDS

88917-11-7Downstream Products

88917-11-7Relevant academic research and scientific papers

Acetylenyl-pyrazolo-pyrimidine derivatives

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Page/Page column 27, (2008/06/13)

The present invention relates to compounds of formula (I): wherein R1 to R3, A, M, L, E, G, and J are as defined in the description and claims. The invention also relates to a process for the manufacture of such compounds, pharmaceutical compositions containing them, and methods for treating CNS disorders.

Acyl sulfonamide anti-proliferatives. Part 2: Activity of heterocyclic sulfonamide derivatives

Mader, Mary M.,Shih, Chuan,Considine, Eileen,De Dios, Alfonso,Grossman, Cora Sue,Hipskind, Philip A.,Lin, Ho-Shen,Lobb, Karen L.,Lopez, Beatriz,Lopez, Jose E.,Cabrejas, Luisa M. Martin,Richett, Michael E.,White, Wesley T.,Cheung, Yiu-Yin,Huang, Zhongping,Reilly, John E.,Dinn, Sean R.

, p. 617 - 620 (2007/10/03)

The anti-proliferative activity of acylated heterocyclic sulfonamides is described in Vascular Endothelial Growth Factor-dependent Human Umbilical Vascular Endothelial Cells (VEGF-HUVEC) and in HCT116 tumor cells in a soft agar diffusion assay.

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