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73188-53-1

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73188-53-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73188-53-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,1,8 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 73188-53:
(7*7)+(6*3)+(5*1)+(4*8)+(3*8)+(2*5)+(1*3)=141
141 % 10 = 1
So 73188-53-1 is a valid CAS Registry Number.

73188-53-1SDS

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-phenylsulfanylhexylsulfanylbenzene

1.2 Other means of identification

Product number -
Other names Hexanal-diphenyldithioacetal

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:73188-53-1 SDS

73188-53-1Relevant articles and documents

An indium-TMSCl promoted reaction of diphenyl diselenide and diorganyl disulfides with aldehydes: novel routes to selenoacetals, thioacetals and alkyl phenyl selenides

Ranu, Brindaban C.,Saha, Amit,Mandal, Tanmay

experimental part, p. 2072 - 2078 (2009/07/11)

The reactions of diphenyl diselenide and dialkyl disulfides with aldehydes in the presence of In-TMSCl have been investigated. Aliphatic aldehydes provide the corresponding selenoacetals and aromatic aldehydes lead predominantly to benzyl phenyl selenides

Synthesis of Aldehydes from Phenylthiotrimethylsilylmethane

Ager, David J.

, p. 1131 - 1136 (2007/10/02)

Phenylthiotrimethylsilylmethyl-lithium (4) reacts with alkyl halides to give 1-phenylthio-1-trimethylsilylalkanes (5), which can also be prepared by the addition of alkyl-lithium to 1-phenylthio-1-trimethylsilylethene (8), or from bis(phenylthio)acetals (11).The 1-phenylthio-1-trimethylsilylalkanes (5) can be converted into the corresponding aldehyde (15) by oxidation to the sulphoxide (13), thermal rearrangement, and hydrolysis of the resultant O-silyl thioacetal (14).

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