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7205-95-0

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7205-95-0 Usage

Appearance

Yellow crystalline solid

Usage

Building block in the synthesis of various organic compounds

Formation

Reaction of chloromethyl methyl sulfide and 4-nitrobenzoyl chloride

Applications

Production of pharmaceuticals and agricultural chemicals

Hazards

Potentially harmful when exposed to skin, eyes, or ingested

Reactivity

Should be handled and used with caution due to its reactivity

Physical state

Solid

Color

Yellow

Chemical structure

Contains a chloromethylsulfinyl group and a nitro group attached to a benzene ring

Check Digit Verification of cas no

The CAS Registry Mumber 7205-95-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,0 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7205-95:
(6*7)+(5*2)+(4*0)+(3*5)+(2*9)+(1*5)=90
90 % 10 = 0
So 7205-95-0 is a valid CAS Registry Number.

7205-95-0SDS

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 1-(chloromethylsulfinyl)-4-nitrobenzene

1.2 Other means of identification

Product number -
Other names Chlormethyl-p-nitrophenyl-sulfoxid

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:7205-95-0 SDS

7205-95-0Relevant articles and documents

Facile Synthesis of α-Chlorosulfoxide Using the N,N'-Dichloro-p-toluenesulfonamide

Kim, Yong Hae,Lim, Sang Chul,Kim, Hyoung Rae,Yoon, Dae Chul

, p. 79 - 82 (2007/10/02)

Various unsymmetrical and symmetrical dialkyl sulfoxides or alkyl aryl sulfoxides reacted with N,N'-dichloro-p-toluenesulfonamide to yield the corresponding α-chlorosulfoxide in excellent yields under mild and neutral conditions in high regioselectivity of monochlorination at α-position of sulfoxides.

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