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

129076-78-4

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129076-78-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129076-78-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,0,7 and 6 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 129076-78:
(8*1)+(7*2)+(6*9)+(5*0)+(4*7)+(3*6)+(2*7)+(1*8)=144
144 % 10 = 4
So 129076-78-4 is a valid CAS Registry Number.

129076-78-4SDS

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-ethyl-N-(2-hydroxy-1-methyl-2,2-diphenylethyl)acetamide

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:129076-78-4 SDS

129076-78-4Downstream Products

129076-78-4Relevant academic research and scientific papers

Photoreduction of aryl ketones by amides, lactams and various nitrogen-containing heterocycles

Gramain, Jean-Claude,Jeandrau, Jean-Pierre,Lemaire, Jacques,Remuson, Roland

, p. 325 - 331 (2007/10/02)

Benzophenone is photoreduced by amides and lactams.The hydrogen atom α to the nitrogen atom is abstracted regioselectively; coupling of the two resulting radicals leads to adducts with a 1-phenylethanolamide structure.The use of this general reaction in synthetic reactions is demonstrated: adducts of benzophenone with amides, lactams, 2,4-imidazolinediones, tetrahydro-2H-1,3-oxazin-2-one and 2-oxazolidinone, and of dibenzosuberone, 9H-xanthenone, 9H-thioxanthenone and α-tetralone with 1-methyl-2-pyrrolidinone, N,N-dimethylacetamide and N,N-diethylacetamide are described.Kinetic parameters for dibenzosuberone and 9H-thioxanthenone are given.Knowledge of the rate constants of photoreduction (kr) and autodeactivation (kTa) allows optimization of the experimental procedure to provide adducts in good yields.

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