Cas 213467-20-0,(E)-(S)-3-[(3,4-Dimethoxy-benzyl)-((R)-1-phenyl-ethyl)-amino]-hex-4-enoic acid methyl ester

213467-20-0

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Basic information

Product Name: (E)-(S)-3-[(3,4-Dimethoxy-benzyl)-((R)-1-phenyl-ethyl)-amino]-hex-4-enoic acid methyl ester
Synonyms: (E)-(S)-3-[(3,4-Dimethoxy-benzyl)-((R)-1-phenyl-ethyl)-amino]-hex-4-enoic acid methyl ester
CAS NO:213467-20-0
Molecular Formula:
Molecular Weight: 397.514
EINECS: N/A
Product Categories: N/A
Mol File: 213467-20-0.mol
Article Data: 1

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: (E)-(S)-3-[(3,4-Dimethoxy-benzyl)-((R)-1-phenyl-ethyl)-amino]-hex-4-enoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (E)-(S)-3-[(3,4-Dimethoxy-benzyl)-((R)-1-phenyl-ethyl)-amino]-hex-4-enoic acid methyl ester(213467-20-0)
EPA Substance Registry System: (E)-(S)-3-[(3,4-Dimethoxy-benzyl)-((R)-1-phenyl-ethyl)-amino]-hex-4-enoic acid methyl ester(213467-20-0)

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: 213467-20-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 213467-20-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,3,4,6 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 213467-20:
(8*2)+(7*1)+(6*3)+(5*4)+(4*6)+(3*7)+(2*2)+(1*0)=110
110 % 10 = 0
So 213467-20-0 is a valid CAS Registry Number.

213467-20-0Upstream product

689-89-4 (2E,4E)-methylhexa-2,4-dienoate

213467-20-0Downstream Products

213467-21-1 (E)-(S)-3-((R)-1-Phenyl-ethylamino)-hex-4-enoic acid methyl ester

213467-20-0Relevant articles and documents

Selective deprotection strategies to N-(α-methylbenzyl)-β-amino esters and derived β-lactams

Davies, Stephen G.,Ichihara, Osamu

, p. 6045 - 6048 (1998)

A variety of N,N-diprotected β-amino esters, prepared by highly diastereoselective conjugate addition of chiral lithium amides, were selectively mono-deprotected under either reductive (hydrogenolysis) or oxidative (DDQ or CAN) conditions. Combined with t

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