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Benzene, 1-chloro-4-[(chloromethyl)sulfonyl]-2-nitro-, also known as 1-Chloro-4-(chloromethylsulfonyl)-2-nitrobenzene, is an organic compound with the chemical formula C7H5Cl2NO3S. It is a derivative of benzene, featuring a chlorine atom at the 1st position, a nitro group at the 2nd position, and a chloromethylsulfonyl group at the 4th position. Benzene, 1-chloro-4-[(chloromethyl)sulfonyl]-2-nitro- is characterized by its potential reactivity and is used in various chemical synthesis processes, particularly in the production of pharmaceuticals and agrochemicals. Due to its complex structure and reactive groups, it is important to handle this chemical with care, adhering to proper safety protocols to minimize potential hazards.

7592-97-4

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7592-97-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7592-97-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,9 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7592-97:
(6*7)+(5*5)+(4*9)+(3*2)+(2*9)+(1*7)=134
134 % 10 = 4
So 7592-97-4 is a valid CAS Registry Number.

7592-97-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-4-(chloromethylsulfonyl)-2-nitrobenzene

1.2 Other means of identification

Product number -
Other names 2-nitro-4-chloromethylsulfonylchlorobenzene

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:7592-97-4 SDS

7592-97-4Relevant academic research and scientific papers

Synthesis and in vitro antibacterial activity of 5-halogenomethylsulfonyl- benzimidazole and benzotriazole derivatives

Ochal, Zbigniew,Bretner, Maria,Wolinowska, Renata,Tyski, Stefan

, p. 1129 - 1136 (2014/01/06)

A series of 5-halogenomethylsulfonylbenzimidazole and benzotriazole derivatives was synthesized as potential antibacterial agents. A new method of synthesis of benzimidazoles was developed. The antimicrobial activities of these compounds were tested against a series of reference and clinical strains. The reference strains include Gram-positive bacteria (S. aureus, S. epidermidis, B. subtilis, B. cereus, E. hirae, M. luteus) and Gram-negative rods (E. coli, P. vulgaris, P. aeruginosa, B. bronchiseptica). The clinical strains include six methicillin-resistant (MRSA) and two methicillin-sensitive (MSSA) S. aureus strains, one methicillin-resistant S. epidermidis, three E. faecalis and two E. faecium strains. Compound with trifluoromethyl- substituent at C-2 position (4) displayed significant antibacterial activities comparable with nitrofurantoin against four strains, and higher against Micrococcus luteus. MIC values for clinical Staphylococci strains (MRSA) were 12.5-25 μg/mL; for Enterococcus strains these values were 50-100 μg/mL. MIC values for reference and clinical strains of Staphylococcus and Enterococcus group were similar, respectively.

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