Cas 515160-09-5,Benzenepropanoic acid, 3,5-dibromo-b-hydroxy-a-methylene-2-(phenylmethoxy)-, methyl ester

515160-09-5

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Basic information

Product Name: Benzenepropanoic acid, 3,5-dibromo-b-hydroxy-a-methylene-2-(phenylmethoxy)-, methyl ester
Synonyms:
CAS NO:515160-09-5
Molecular Formula: C18H16Br2O4
Molecular Weight: 456.131
EINECS: N/A
Product Categories: N/A
Mol File: 515160-09-5.mol
Article Data: 2

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, 3,5-dibromo-b-hydroxy-a-methylene-2-(phenylmethoxy)-, methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzenepropanoic acid, 3,5-dibromo-b-hydroxy-a-methylene-2-(phenylmethoxy)-, methyl ester(515160-09-5)
EPA Substance Registry System: Benzenepropanoic acid, 3,5-dibromo-b-hydroxy-a-methylene-2-(phenylmethoxy)-, methyl ester(515160-09-5)

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: 515160-09-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 515160-09-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,5,1,6 and 0 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 515160-09:
(8*5)+(7*1)+(6*5)+(5*1)+(4*6)+(3*0)+(2*0)+(1*9)=115
115 % 10 = 5
So 515160-09-5 is a valid CAS Registry Number.

515160-09-5Upstream product

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515160-09-5Relevant articles and documents

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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