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N-(2-oxo-1,2-diphenylethyl)propionamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

135120-34-2

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135120-34-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135120-34-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,1,2 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 135120-34:
(8*1)+(7*3)+(6*5)+(5*1)+(4*2)+(3*0)+(2*3)+(1*4)=82
82 % 10 = 2
So 135120-34-2 is a valid CAS Registry Number.

135120-34-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-oxo-1,2-diphenylethyl)propionamide

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:135120-34-2 SDS

135120-34-2Relevant academic research and scientific papers

Catalytic transformation of esters of 1,2-azido alcohols into α-amido ketones

Kim, Yongjin,Pak, Han Kyu,Rhee, Young Ho,Park, Jaiwook

supporting information, p. 6549 - 6552 (2016/06/01)

The esters of 1,2-azido alcohols were transformed into α-amido ketones without external oxidants through the Ru-catalyzed formation of N-H imines with the liberation of N2 followed by intramolecular migration of the acyl moiety. A wide range of α-amido ketones were obtained, and one-pot transformation into the corresponding oxazoles (or a thiazole) was demonstrated.

REACTION OF HYDROXYMETHYL ARYL KETONES WITH AROMATIC HYDROCARBONS

Bal'on, Ya. G.,Smirnov, V. A.

, p. 1712 - 1715 (2007/10/02)

The readily obtainable products from the condensation of arylglyoxals with carboxamides react with benzene and its analogs in the presence of concentrated sulfuric acid or phosphorus pentoxide in trifluoroacetic acid with the formation of arylmethyl aryl ketones, which are used for the synthesis of substituted azoles.

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