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Benzenepropanamide, b-hydroxy-N-methyl-a-1-propenyl-, also known as N-Methyl-2-(1-propenyl)-3-phenylpropionamide, is a chemical compound with the molecular formula C12H17NO. It is a derivative of benzenepropanamide, featuring a hydroxyl group at the beta position, a methyl group at the nitrogen atom, and a propenyl group at the alpha position. Benzenepropanamide, b-hydroxy-N-methyl-a-1-propenyl- is an organic molecule with potential applications in pharmaceuticals and chemical synthesis, particularly as an intermediate in the production of various drugs and other organic compounds. Its structure and properties make it a versatile building block in the synthesis of more complex molecules, highlighting its importance in the field of organic chemistry.

142541-19-3

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142541-19-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 142541-19-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,5,4 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 142541-19:
(8*1)+(7*4)+(6*2)+(5*5)+(4*4)+(3*1)+(2*1)+(1*9)=103
103 % 10 = 3
So 142541-19-3 is a valid CAS Registry Number.

142541-19-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (R,R:S,S)-1-Methyl-2-(hydroxybenzyl)-3-pentenamide

1.2 Other means of identification

Product number -
Other names (E)-2-(Hydroxy-phenyl-methyl)-pent-3-enoic acid methylamide

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:142541-19-3 SDS

142541-19-3Downstream Products

142541-19-3Relevant academic research and scientific papers

Stereoselective syntheses of substituted 5,6-dihydro-2(1H)-pyridinones in polyphosphate media

Marson,Grabowska,Fallah,Walsgrove,Eggleston,Baures

, p. 291 - 296 (2007/10/02)

δ-Lactams have been synthesized with excellent stereocontrol of substituents by condensing 3-alkenamides with aryl aldehydes in polyphosphoric ester. The scope of the condensation of 3-alkenamides with aryl aldehydes in several phosphate media is examined, and a rationale is proposed regarding γ-lactam versus δ-lactam formation.

Stereocontrolled Syntheses of Substituted Unsaturated δ-Lactams from 3-Alkenamides

Marson, Charles M.,Grabowska, Urszula,Walsgrove, Timothy

, p. 5045 - 5047 (2007/10/02)

δ-Lactams have been synthesized with excellent stereocontrol of substituents by condensing 3-alkenamides with aryl aldehydes in polyphosphoric ester.

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