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Phosphonothioic diamide, N,N-diethyl-N',N'-dimethyl-P-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

132573-80-9

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132573-80-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132573-80-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,5,7 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 132573-80:
(8*1)+(7*3)+(6*2)+(5*5)+(4*7)+(3*3)+(2*8)+(1*0)=119
119 % 10 = 9
So 132573-80-9 is a valid CAS Registry Number.

132573-80-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[benzyl(dimethylamino)phosphinothioyl]-N-ethylethanamine

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:132573-80-9 SDS

132573-80-9Downstream Products

132573-80-9Relevant academic research and scientific papers

Nucleophilic Substitution in Benzylic Phosphonamidothioic Chlorides: Influence of Substituents on the Elimination-Addition Pathway

Harger, Martin J. P.,Hurman, Barbara T.

, p. 490 - 491 (2007/10/03)

The elimination-addition pathway that competes with SN2(P) in the reaction of ArCH2P(S)(NMe2)CI with Et2NH is very sensitive to the acidity of the benzylic C - H bond (p 3.45).

Nucleophilic Substitution in Benzylic Thiophosphinyl and Thiophosphonyl Chlorides: the Contribution of Elimination-Addition Pathways with Methylenethiooxophosphorane (Thiophosphene) Intermediates

Coogan, Michael P.,Harger, Martin J. P.

, p. 2101 - 2108 (2007/10/02)

For the reactions of ArCH2P(S)(Ph)Cl and ArCH2P(S)(NMe2)Cl with Et2NH, changing ArCH2 from benzyl to 4-nitrobenzyl increases the rates of substitution by factors of 80 and >103, respectively, and reduces markedly the ability to discriminate bet

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