574746-36-4

Basic information

• Product Name: Benzenepropanoic acid, b-hydroxy-2-(phenylmethoxy)-a-[[(phenylmethyl)amino]methyl]-, methyl ester
• CAS NO: 574746-36-4
• Molecular Formula: C25H27NO4
• Molecular Weight: 405.494
• Mol File: 574746-36-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzenepropanoic acid, b-hydroxy-2-(phenylmethoxy)-a-[[(phenylmethyl)amino]methyl]-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenepropanoic acid, b-hydroxy-2-(phenylmethoxy)-a-[[(phenylmethyl)amino]methyl]-, methyl ester(574746-36-4)
• EPA Substance Registry System: Benzenepropanoic acid, b-hydroxy-2-(phenylmethoxy)-a-[[(phenylmethyl)amino]methyl]-, methyl ester(574746-36-4)

Safety Data

• Hazardous Substances Data: 574746-36-4(Hazardous Substances Data)

Upstream product

• 153333-22-3 methyl 3-(2-benzyloxyphenyl)-3-hydroxy-2-methylene propanoate 
• 100-46-9 benzylamine 
• 5896-17-3 2-(phenylmethoxy)benzaldehyde 

Downstream Products

• 2445-82-1 3-methylcoumarine 

Relevant articles and documents

Application of Baylis-Hillman methodology in the synthesis of coumarin derivatives

A general, chemoselective approach to 3-substituted coumarins via Baylis-Hillman reactions of O-benzylated salicylaldehyde precursors has been demonstrated. Competitive cyclization to chromene derivatives is inhibited by conjugate addition of benzylamine or piperidine to the α,β-unsaturated ester intermediates.