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59036-45-2

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59036-45-2 Usage

General Description

The chemical compound {[(2E)-3-chloroprop-2-en-1-yl]sulfanyl}benzene is an organosulfur compound that contains a benzene ring with a thiol group attached to it. The molecule also contains a 3-chloroprop-2-ene group, which is a type of olefin. {[(2E)-3-chloroprop-2-en-1-yl]sulfanyl}benzene can be used in organic synthesis and as a building block for creating more complex organic molecules. It may also have potential applications in the pharmaceutical and agricultural industries. Additionally, its structural features make it a candidate for various chemical reactions, including substitution and addition reactions. Overall, this chemical has potential usefulness in the laboratory and industrial settings for its unique structure and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 59036-45-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,0,3 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 59036-45:
(7*5)+(6*9)+(5*0)+(4*3)+(3*6)+(2*4)+(1*5)=132
132 % 10 = 2
So 59036-45-2 is a valid CAS Registry Number.

59036-45-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name [(E)-3-chloroprop-2-enyl]sulfanylbenzene

1.2 Other means of identification

Product number -
Other names 1c-Chlor-3-phenylmercapto-propen

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:59036-45-2 SDS

59036-45-2Relevant articles and documents

Effect of chalcogenyl substituent on the course of allyl rearrangement at chalcogenation of 1,3-dichloropropene

Levanova,Nikonova,Grabel’nykh,Russavskaya,Albanov,Rozentsveig,Korchevin

, p. 615 - 623 (2016/07/06)

Formation of 1,3-dichalcogenylpropene at the treatment of 1,3-dichloropropene with organic dichalcogenides in a redox system hydrazine hydrate–KOH is governed by the possibility of an allyl rearrangement. In the presence of bases this rearrangement proceeds via carbanion partially stabilized by the chalcogenyl substituent. The effectivity of the stabilization and consequently the probability of the rearrangement varies in the series of substituents PhS > BnS > PhSe. In the stage of the direct nucleophilic substitution of chlorine the anion PhSe?possesses the highest activity.

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