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141312-50-7

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141312-50-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141312-50-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,3,1 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 141312-50:
(8*1)+(7*4)+(6*1)+(5*3)+(4*1)+(3*2)+(2*5)+(1*0)=77
77 % 10 = 7
So 141312-50-7 is a valid CAS Registry Number.

141312-50-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenyl-N-propan-2-yl-N-propylacetamide

1.2 Other means of identification

Product number -
Other names Benzeneacetamide,N-(1-methylethyl)-N-propyl

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:141312-50-7 SDS

141312-50-7Downstream Products

141312-50-7Relevant articles and documents

CONFORMATIONS IN UNSYMMETRICALLY N-n-PROPYL-N-SUBSTITUTED 2-PHENYLACETAMIDES

Antonovic, D. G.,Vajs, V. E.,Stojanovic, N. D.,Nikolic, A. D.,Petrovic, S. D.

, p. 255 - 258 (2007/10/02)

As a part of a study on the structural characteristics of some new various N-alkyl-N-substituted 2-phenylacetamides the infrared and 1H N.M.R. spectra were obtained and interpreted.The synthesis of a various N-n-propyl-N-alkyl 2-phenylacetamides of the general formula PhCH2CON(nPr)R, wherein R is ethyl, isopropyl, n-butyl, t-butyl and cyclohexyl, were performed.The corresponding mixed secondary amines of the type HNnPrR were obtained by catalytic hydrogenation of the synthetized propylidenealkylamines.The 1H N.M.R. spectra of these unsymmetrically N,N-disubstituted amides have been studied and the peaks have been assigned in each cases to two possible conformational isomers, arising from the lack of free rotation about the C(O)-N bond.These results are in accordance with our previous investigation of the structure of N-substituted 2-phenylacetamides.

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