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736137-64-7

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736137-64-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 736137-64-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,6,1,3 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 736137-64:
(8*7)+(7*3)+(6*6)+(5*1)+(4*3)+(3*7)+(2*6)+(1*4)=167
167 % 10 = 7
So 736137-64-7 is a valid CAS Registry Number.

736137-64-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-2-[(5-methyl-2-sulfanylphenyl)phosphanyl]benzenethiol

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:736137-64-7 SDS

736137-64-7Downstream Products

736137-64-7Relevant articles and documents

Identification of a four-center intermediate in a Grignard addition reaction to a P-S bond

Baccolini, Graziano,Boga, Carla,Mazzacurati, Marzia

, p. 12595 - 12600 (2008/03/14)

The reaction between tert-butylmagnesium chloride (or tert-pentylmagnesium chloride) and the particular phosphorus-sulfur bond of a benzothiadiphospholic system showed, for the first time, evidence of formation of intermediates with a four-center structure. The possibility, for the phosphorus atom, to have very stable hypervalent coordinations makes it possible to observe its hypervalent states during the course of a reaction. The benzothiadiphosphole, with its bicyclic folded structure, further stabilizes the hypervalent coordinations thus making the intermediates sufficiently stable to be detected during the course of the reaction by 31P NMR spectroscopy, which revealed the nature and the stability of the species involved in this reaction, carried out also using other Grignard reagents.

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