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19552-12-6

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19552-12-6 Usage

Appearance

Yellow crystalline solid

Solubility

Insoluble in water, soluble in organic solvents

Uses

a. Synthesis of organic compounds
b. Intermediate in the production of dyes and pigments

Odor

Strong

Toxicity

Toxic, harmful effects on human health if ingested, inhaled, or in contact with skin

Environmental hazard

Potential negative impacts on aquatic organisms

Safety measures

Handle and store with care, 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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