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51310-28-2

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51310-28-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51310-28-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,3,1 and 0 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 51310-28:
(7*5)+(6*1)+(5*3)+(4*1)+(3*0)+(2*2)+(1*8)=72
72 % 10 = 2
So 51310-28-2 is a valid CAS Registry Number.

51310-28-2SDS

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 N-(2-methyl-1-phenylpropan-2-yl)benzamide

1.2 Other means of identification

Product number -
Other names 2-Benzamino-2-methyl-1-phenyl-propan

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:51310-28-2 SDS

51310-28-2Downstream Products

51310-28-2Relevant articles and documents

Polyvinylpolypyrrolidone-supported boron trifluoride: A high-loaded, polymer-supported Lewis acid for the Ritter reaction

Lakouraj, Moslem Mansour,Mokhtary, Masoud

experimental part, p. 53 - 56 (2010/03/30)

A Mild and efficient method for preparing amides by reaction of nitriles with benzhydrol and tertiary alcohols is described using polyvinylpolypyrrolidone-supported boron trifluoride. Selective amidation of benzhydrol in the presence of primary benzyl alcohols was also achieved.

Evolutions differentes de radicaux anions formes par voie chimique ou electrochimique

Archier-Jay, Danielle,Besbes, Neji,Laurent, Andre,Laurent, Eliane,Lesniak, Stanislaw,Tardivel, Robert

, p. 537 - 543 (2007/10/02)

Chemical and electrochemical reductions of N-aroylaziridines 1 are described and compared.The first step is a single electron transfer (1 +e -> 1-. -> 1'-.).But compounds obtained from 1'-. are depending on the method used way followed: chemical reduction of N-cinnamoylaziridine 1e provides pyrrolidone 10e; but oxazoline 11e is available by electrochemical reduction of the same starting material 1e.Counter ion seems responsible of these different results.In agreement with this hypothesis, it is shown that pyrrolidone 10e is obtained from 1j only in presence of a counter ion.

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