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19552-12-6

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19552-12-6 Usage

General Description

1-[(4-methylbenzyl)sulfanyl]-2,4-dinitrobenzene is a chemical compound with the molecular formula C14H12N2O4S. It is a yellow crystalline solid that is insoluble in water but soluble in organic solvents. 1-[(4-methylbenzyl)sulfanyl]-2,4-dinitrobenzene is used in the synthesis of organic compounds and as an intermediate in the production of dyes and pigments. It has a strong odor and is considered to be toxic, with potential harmful effects on human health if ingested, inhaled, or in contact with skin. The compound is also classified as an environmental hazard, with potential negative impacts on aquatic organisms. Therefore, it should be handled and stored with care, and appropriate safety measures should be taken when working with this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 19552-12-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,5,5 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 19552-12:
(7*1)+(6*9)+(5*5)+(4*5)+(3*2)+(2*1)+(1*2)=116
116 % 10 = 6
So 19552-12-6 is a valid CAS Registry Number.

19552-12-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(4-methylphenyl)methylsulfanyl]-2,4-dinitrobenzene

1.2 Other means of identification

Product number -
Other names Sulfide,2,4-dinitrophenyl p-methylbenzyl

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:19552-12-6 SDS

19552-12-6Downstream Products

19552-12-6Relevant articles and documents

Co-C bond cleavage in the reactions of alkyl, benzyl and heteroaromaticmethyl cobaloximes with arene sulfenyl chloride: Homolytic and heterolytic pathways

Gupta,Dixit, Vandana,Das, Indira

, p. 49 - 58 (2007/10/03)

The reactions of arene sulfenyl chlorides, ArSCl, (Ar=Ph, C6Cl5, 2,4 (NO2)2C6H3) with organocobaloximes, RCo(dmgH)2Py, (R=alkyl, benzyl and heteroaromaticmethyl) were carried out under thermal and photochemical conditions. A variety of organic and organometallic products are formed depending upon the substrate cobaloxime. For 3-methoxybenzyl and heteroaromaticmethyl cobaloximes the results suggest that they represent a unique class of cobaloximes whereby both the aromatic ring as well as the Co-C bond are highly activated towards attack by the arene sulfenyl chloride. Both homolytic as well as heterolytic pathways are operative.

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