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1-Butanesulfenyl chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14925-97-4

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14925-97-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14925-97-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,9,2 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 14925-97:
(7*1)+(6*4)+(5*9)+(4*2)+(3*5)+(2*9)+(1*7)=124
124 % 10 = 4
So 14925-97-4 is a valid CAS Registry Number.

14925-97-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name butyl thiohypochlorite

1.2 Other means of identification

Product number -
Other names thiohypochlorous acid butyl ester

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:14925-97-4 SDS

14925-97-4Relevant academic research and scientific papers

A MILD AND CONVENIENT PREPARATION OF SULFENYL CHLORIDES FROM THIOLACETATES

Thea, Sergio,Cevasco, Giorgio

, p. 2865 - 2866 (2007/10/02)

Sulfenyl chlorides are obtained easily and in good yields through the reaction of thiolesters and sulfuryl chloride.

SYNTHESIS OF DICHLOROKETENE ACETALS UNDER CONDITIONS OF PHASE-TRANSFER CATALYSIS AND THEIR REACTIONS WITH SULFUR-CONTAINING ELECTROPHILES

Guseva, S. A.,Mirskova, A. N.,Levkovskaya, G. G.,Kalikhman, I. D.,Voronkov, M. G.

, p. 261 - 268 (2007/10/02)

A method was developed for the production of dichloroketene acetals by the dehydrochlorination of chloral acetals in DMFA in the presence of triethylbenzylammonium chloride as phase-transfer catalyst.Sulfur monochloride, sulfur dichloride, and benzene sulfenyl chloride react with dichloroketene acetals with the formation of adducts (alkoxycarbonyldichloromethanesulfenyl chloride ClSCCl2COOR, alkoxycarbonyldichloromethanethiosulfenyl chloride ClSSCCl2COOR, and butyl phenylthiodichloroacetate C6H5SCCl2COOR respectively).The action of secondary amines on butoxycarbonyldichloromethanesulfenyl chloride gave sulfenamides R1R2NSCCl2COOBu.The reactions of butoxycarbonyldichloromethanethiosulfenyl chloride and butyl phenylthiodichloroacetate with secondary amines under various conditions led to degradation products.

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