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2-[(DIFLUOROMETHYL)THIO]ANILINE HYDROCHLORIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24933-58-2

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24933-58-2 Usage

Molecular weight

189.66 g/mol

Organic compound

Yes

Commonly used in

Pharmaceutical and agrochemical industries

Physical form

White to off-white solid

Melting point

180-183°C

Solubility

Soluble in water

Use

Intermediate for the synthesis of various compounds

Safety precautions

Handle with care and follow proper safety precautions in a laboratory setting.

Check Digit Verification of cas no

The CAS Registry Mumber 24933-58-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,9,3 and 3 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 24933-58:
(7*2)+(6*4)+(5*9)+(4*3)+(3*3)+(2*5)+(1*8)=122
122 % 10 = 2
So 24933-58-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H7F2NS/c8-7(9)11-6-4-2-1-3-5(6)10/h1-4,7H,10H2

24933-58-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(difluoromethylsulfanyl)aniline,hydrochloride

1.2 Other means of identification

Product number -
Other names 2-(difluoromethylsulfanyl)aniline

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:24933-58-2 SDS

24933-58-2Downstream Products

24933-58-2Relevant academic research and scientific papers

Radical Difluoromethylation of Thiols with (Difluoromethyl)triphenylphosphonium Bromide

Heine, Niklas B.,Studer, Armido

supporting information, p. 4150 - 4153 (2017/08/14)

A method for facile difluoromethylation of various thiols using (difluoromethyl)triphenylphosphonium bromide under mild reaction conditions is presented. The transformation proceeds in the absence of any transition metal using a bench-stable and readily accessible phosphonium salt. Deuterium labeling experiments and cyclic voltammetry measurements reveal that the difluoromethylation occurs via a SRN1-type mechanism. Substrate scope is broad, and various functional groups are tolerated (OH, NH2, amide, ester).

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