Cas 164660-15-5,(R)-3-[Allyl-((S)-1-phenyl-ethyl)-amino]-3-phenyl-propionic acid tert-butyl ester

164660-15-5

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Basic information

Product Name: (R)-3-[Allyl-((S)-1-phenyl-ethyl)-amino]-3-phenyl-propionic acid tert-butyl ester
Synonyms: (R)-3-[Allyl-((S)-1-phenyl-ethyl)-amino]-3-phenyl-propionic acid tert-butyl ester
CAS NO:164660-15-5
Molecular Formula:
Molecular Weight: 365.516
EINECS: N/A
Product Categories: N/A
Mol File: 164660-15-5.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: (R)-3-[Allyl-((S)-1-phenyl-ethyl)-amino]-3-phenyl-propionic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (R)-3-[Allyl-((S)-1-phenyl-ethyl)-amino]-3-phenyl-propionic acid tert-butyl ester(164660-15-5)
EPA Substance Registry System: (R)-3-[Allyl-((S)-1-phenyl-ethyl)-amino]-3-phenyl-propionic acid tert-butyl ester(164660-15-5)

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: 164660-15-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 164660-15-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,6,6 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 164660-15:
(8*1)+(7*6)+(6*4)+(5*6)+(4*6)+(3*0)+(2*1)+(1*5)=135
135 % 10 = 5
So 164660-15-5 is a valid CAS Registry Number.

164660-15-5Upstream product

164660-15-5Downstream Products

146937-36-2 tert-butyl (3R,αS)-3-[N-(α-methylbenzyl)amino]-3-phenylpropanoate

164660-15-5Relevant articles and documents

Lithium (α-Methylbenzyl)allylamide: A Differentially Protected Chiral Ammonia Equivalent for the Asymmetric Synthesis of β-Amino Acids and β-Lactams

Davies, Stephen G.,Fenwick, David R.

, p. 1109 - 1110 (1995)

The addition products from the highly stereoselective conjugate additions of lithium (αS)-(α-methylbenzyl)allylamide to α,β-unsaturated tert-butyl esters are efficiently deallylated with tris(triphenylphosphine)rhodium(I) chloride and converted, after tra

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