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87453-67-6

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87453-67-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87453-67-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,4,5 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 87453-67:
(7*8)+(6*7)+(5*4)+(4*5)+(3*3)+(2*6)+(1*7)=166
166 % 10 = 6
So 87453-67-6 is a valid CAS Registry Number.

87453-67-6SDS

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 1,2-bis(propylsulfanyl)benzene

1.2 Other means of identification

Product number -
Other names 1,2-bis(propylthio)benzene

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:87453-67-6 SDS

87453-67-6Downstream Products

87453-67-6Relevant articles and documents

Metallation reactions. XXVI. α,α'-Dimetallation of 1,2-bis (methylthiobenzene)

Cabiddu,Cabiddu,Cadoni,De Montis,Fattuoni,Melis,Sotgiu

, p. 14069 - 14078 (2007/10/03)

Dimetallation of bis(methylthio)benzene (1) with butyllithium or with superbases gives 2 with good yield. This species allows the simultaneous introduction of two electrophiles in thiomethyl groups. Alternatively it was possible to functionalize these gro

Process for the nucleophilic substitution of unactivated aromatic and heteroaromatic substrates

-

, (2008/06/13)

The nucleophilic substitution upon unactivated monocyclic or polycyclic aromatic or heteroaromatic substrates bearing suitable leaving groups can be achieved by catalyzing the substitution of said leaving groups by an anionic nucleophile with a cyclic or acyclic polydentate chelating ligand. Specific products of this reaction can be used in preparing sulfonylurea herbicides.

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