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4153-06-4

Benzenesulfenyl chloride, 4-chloro-2-nitro-, also known as 2-(4-chlorophenylsulfenyl)-1-nitrobenzene, is an organic compound with the chemical formula C12H8ClNO2S. It is a yellow crystalline solid that is soluble in organic solvents. Benzenesulfenyl chloride, 4-chloro-2-nitro- is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is characterized by its unique structure, which includes a benzene ring with a sulfenyl chloride group attached to one carbon atom and a nitro group attached to an adjacent carbon atom. The presence of both a sulfenyl chloride and a nitro group in the molecule makes it a versatile building block for the development of new chemical entities with potential applications in various industries.

4153-06-4

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4153-06-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4153-06-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,5 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4153-06:
(6*4)+(5*1)+(4*5)+(3*3)+(2*0)+(1*6)=64
64 % 10 = 4
So 4153-06-4 is a valid CAS Registry Number.

4153-06-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-chloro-2-nitrophenyl) thiohypochlorite

1.2 Other means of identification

Product number -
Other names chloro-(4-chloro-2-nitro-phenyl)-sulfane

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:4153-06-4 SDS

4153-06-4Relevant articles and documents

Electrophilic cleavage of cyclopropanes. II. Concerning the effect of increasing electron demand upon the product-determining transition state in the reaction of 4-substituted-2-nitrobenzenesulphenyl chlorides and benzenesulphenyl chlorides with tetracyclo2,7.04,6>heptane....

Beaulieu, Pierre L.,Kabo, Ann,Garratt, Dennis G.

, p. 1014 - 1020 (2007/10/02)

The effect of increasing electron demand upon the product-determining transition state in the reaction of arenesulphenyl chlorides with tetracyclo2,7.04,6>heptane has been investigated.As the electron donating ability of the remote substituents on the phenyl ring of the sulphenyl chloride is varied from nitro to methoxy the relative proportion of adducts derived from edge-on attack is found to increase relative to that of adducts derived from corner attack.An ortho-nitro group was found to lead to a stabilizing interaction only in the case of 2,4-dinitrobenzenesulphenyl chloride.A mechanism involving the competition between the two conceptual modes of approach is suggested.

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