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Benzamide, N-[(dichlorofluoromethyl)thio]-, also known as dichlorofluoromethyl thiobenzamide or DCFMB, is a chemical compound with the molecular formula C8H5Cl2FNOS. It is a derivative of benzamide, featuring a dichlorofluoromethylthio group attached to the nitrogen atom. DCFMB is a potent and selective inhibitor of the enzyme cysteine protease, which plays a crucial role in various biological processes. Due to its ability to inhibit cysteine proteases, DCFMB has been studied for its potential applications in the treatment of diseases associated with abnormal protease activity, such as cancer and neurodegenerative disorders. The compound is also used as a reagent in chemical synthesis and as a tool in biochemical research to study the function and regulation of cysteine proteases.

1014-36-4

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1014-36-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1014-36-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,1 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1014-36:
(6*1)+(5*0)+(4*1)+(3*4)+(2*3)+(1*6)=34
34 % 10 = 4
So 1014-36-4 is a valid CAS Registry Number.

1014-36-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(Dichloro-fluoro-methylsulfanyl)-benzamide

1.2 Other means of identification

Product number -
Other names -

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

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More Details:1014-36-4 SDS

1014-36-4Relevant academic research and scientific papers

IMINATION OF SULFUR-CONTAINING COMPOUNDS. XVI. ARYLSULFONYLIMINATION OF N-SUBSTITUTED HALOGENOMETHANESULFENAMIDES

Koval', I.V.,Tarasenko, A.I.,Kremlev, M.M.,Molchanova, N.R.

, p. 452 - 457 (2007/10/02)

In the reaction of sodiochloroamides of sulfonic acids with N-acylmethanesulfenamides, in addition to imination of the latter, the S-N bond is cleaved and the CH3S residue is iminated.It was shown that the ability of N-acylhalogenomethanesulfenamides to be iminated by the sodiochloroamides of sulfonic acids may be due to the acidic characteristics of the compounds and also to steric factors.N-Acyl-N'-aryl(alkyl)sulfonyldichlorofluoromethanesulfenamidines and the corresponding difluorochloromethanesulfenamidines were obtained by the imination of N-acyldichlorofluoromethanesulfenamides and the corresponding difluorochloromethanesulfenamides by sodiochloroamides of sulfonic acids, and their acidic characteristics were studied.

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