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5038-59-5

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5038-59-5 Usage

General Description

4-(2-bromoacetyl)benzenesulfonyl chloride, also known as 2-(4-Chlorosulfonylphenyl)-2-bromopropanoic acid, is a synthetic organic compound. It falls under the category of organosulfur compounds and features a benzene ring. Its chemical formula is C8H6BrClO3S. 4-(2-Bromoacetyl)benzenesulfonyl chloride is typically used in research and development settings, in particular within organic synthesis processes as it can be used to produce other complex chemical compounds. Handle with care as it may be harmful if swallowed, inhaled or in contact with skin. The long-term effects of exposure to this chemical on human health and the environment are not fully understood.

Check Digit Verification of cas no

The CAS Registry Mumber 5038-59-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,3 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5038-59:
(6*5)+(5*0)+(4*3)+(3*8)+(2*5)+(1*9)=85
85 % 10 = 5
So 5038-59-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H6BrClO3S/c9-5-8(11)6-1-3-7(4-2-6)14(10,12)13/h1-4H,5H2

5038-59-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2-BROMOACETYL)BENZENESULFONYL CHLORIDE

1.2 Other means of identification

Product number -
Other names 4-(2-bromanylethanoyl)benzenesulfonyl 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:5038-59-5 SDS

5038-59-5Relevant articles and documents

Nucleus-independent chemical shift (NICS) as a criterion for the design of new antifungal benzofuranones

González-Chávez, Marco Martín,González-Chávez, Rodolfo,Méndez, Francisco,Martínez, Roberto,Ni?o-Moreno, Perla Del Carmen,Ojeda-Fuentes, Luis Enrique,Richaud, Arlette,Zerme?o-Macías, María de los ángeles

, (2021/08/30)

The assertion made by Wu et al. that aromaticity may have considerable implications for molecular design motivated us to use nucleus-independent chemical shifts (NICS) as an aromaticity criterion to evaluate the antifungal activity of two series of indol-4-ones. A linear regression analysis of NICS and antifungal activity showed that both tested variables were significantly related (p –1 for Candida glabrata, Candida krusei and Candida guilliermondii with compounds 15-32, 15-15 and 15-1. The MIC for filamentous fungi was 1.95 μg·mL–1 for Aspergillus niger for compounds 15-1, 15-33 and 15-34. The results obtained support the use of NICS in the molecular design of compounds with antifungal activity.

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