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2-Propenamide, N-hydroxy-N-(4-methylphenyl)-3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29284-28-4

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29284-28-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29284-28-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,2,8 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 29284-28:
(7*2)+(6*9)+(5*2)+(4*8)+(3*4)+(2*2)+(1*8)=134
134 % 10 = 4
So 29284-28-4 is a valid CAS Registry Number.

29284-28-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-hydroxy-N-(4-methylphenyl)-3-phenylprop-2-enamide

1.2 Other means of identification

Product number -
Other names p-tolylcinnamohydroxamic acid

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:29284-28-4 SDS

29284-28-4Relevant academic research and scientific papers

One-step formation both of C-N and of C-O bonds of N-alkoxyamides through NHC-catalyzed three-component reactions of enals, nitrosoarenes, and enones

Sun, Zhong-Xin,Cheng, Ying

, p. 4982 - 4987 (2013/01/14)

NHC-catalyzed three-component reactions of α,β-unsaturated aldehydes (enals), nitrosoarenes, and α,β-unsaturated ketones (enones) were studied. The reactions proceeded through a cascade aza-benzoin condensation/oxo-Michael addition sequence to produce N,O-bisfunctionalized N-hydroxylacrylamides in moderate to good yields. This work not only provides an efficient method for the one-step formation both of the C-N and of the C-O bonds in N-alkoxyamides, but also advances the application of NHC organocatalysis in the field of multicomponent reactions. NHC-catalyzed three-component reactions of α,β-unsaturated aldehydes (enals), nitrosoarenes, and α,β-unsaturated ketones (enones) proceeded through a cascade aza-benzoin condensation/oxo-Michael addition sequence to produce N,O-bisfunctionalized N-hydroxylacrylamides in moderate to good yields. Copyright

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