Cas 574746-57-9,Benzenepropanoic acid, 3-ethoxy-b-hydroxy-2-(phenylmethoxy)-a-[[(phenylmethyl)amino]methyl]- , methyl ester

574746-57-9

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Basic information

Product Name: Benzenepropanoic acid, 3-ethoxy-b-hydroxy-2-(phenylmethoxy)-a-[[(phenylmethyl)amino]methyl]- , methyl ester
Synonyms:
CAS NO:574746-57-9
Molecular Formula: C27H31NO5
Molecular Weight: 449.547
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Benzenepropanoic acid, 3-ethoxy-b-hydroxy-2-(phenylmethoxy)-a-[[(phenylmethyl)amino]methyl]- , methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzenepropanoic acid, 3-ethoxy-b-hydroxy-2-(phenylmethoxy)-a-[[(phenylmethyl)amino]methyl]- , methyl ester(574746-57-9)
EPA Substance Registry System: Benzenepropanoic acid, 3-ethoxy-b-hydroxy-2-(phenylmethoxy)-a-[[(phenylmethyl)amino]methyl]- , methyl ester(574746-57-9)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 574746-57-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 574746-57-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,7,4,7,4 and 6 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 574746-57:
(8*5)+(7*7)+(6*4)+(5*7)+(4*4)+(3*6)+(2*5)+(1*7)=199
199 % 10 = 9
So 574746-57-9 is a valid CAS Registry Number.

574746-57-9Upstream product

574746-57-9Downstream Products

574746-57-9Relevant academic research and scientific papers

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

Kaye, Perry T.,Musa

, p. 1755 - 1770 (2007/10/03)

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.

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