Cas 893395-89-6,(R)-3-([(R)-2-amino-2-oxo-1-phenylethyl]amino)-3-phenylpropionic acid ethyl ester hydrochloride

893395-89-6

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Basic information

Product Name: (R)-3-([(R)-2-amino-2-oxo-1-phenylethyl]amino)-3-phenylpropionic acid ethyl ester hydrochloride
Synonyms: (R)-3-([(R)-2-amino-2-oxo-1-phenylethyl]amino)-3-phenylpropionic acid ethyl ester hydrochloride
CAS NO:893395-89-6
Molecular Formula:
Molecular Weight: 362.856
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: (R)-3-([(R)-2-amino-2-oxo-1-phenylethyl]amino)-3-phenylpropionic acid ethyl ester hydrochloride(CAS DataBase Reference)
NIST Chemistry Reference: (R)-3-([(R)-2-amino-2-oxo-1-phenylethyl]amino)-3-phenylpropionic acid ethyl ester hydrochloride(893395-89-6)
EPA Substance Registry System: (R)-3-([(R)-2-amino-2-oxo-1-phenylethyl]amino)-3-phenylpropionic acid ethyl ester hydrochloride(893395-89-6)

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: 893395-89-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 893395-89-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,3,3,9 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 893395-89:
(8*8)+(7*9)+(6*3)+(5*3)+(4*9)+(3*5)+(2*8)+(1*9)=236
236 % 10 = 6
So 893395-89-6 is a valid CAS Registry Number.

893395-89-6Upstream product

893395-89-6Downstream Products

3082-68-6 (R)-3-amino-3-phenylpropionic acid ethyl ester

893395-89-6Relevant academic research and scientific papers

PROCESS FOR THE PREPARATION OF CHIRAL AMINES

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Page/Page column 9-10, (2008/06/13)

The invention relates to a process for the preparation of a chiral amine, whereby a ketone or aldehyde is contacted with an enantiomerically enriched phenylglycine amide to give an imine, whereby the imine is subsequently contacted with a Reformatsky reagent and the formed compound is subsequently converted into a chiral amine by means of hydrogenolysis, oxidation or a retro Strecker method.

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