Cas 1332928-72-9,tert-butyl (2S,3R,αS)-2-deuterio-3-[N-benzyl-N-(α-methylbenzyl)amino]-3-(3'-fluorophenyl)propanoate

1332928-72-9

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Basic information

Product Name: tert-butyl (2S,3R,αS)-2-deuterio-3-[N-benzyl-N-(α-methylbenzyl)amino]-3-(3'-fluorophenyl)propanoate
Synonyms: tert-butyl (2S,3R,αS)-2-deuterio-3-[N-benzyl-N-(α-methylbenzyl)amino]-3-(3'-fluorophenyl)propanoate
CAS NO:1332928-72-9
Molecular Formula:
Molecular Weight: 434.558
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: tert-butyl (2S,3R,αS)-2-deuterio-3-[N-benzyl-N-(α-methylbenzyl)amino]-3-(3'-fluorophenyl)propanoate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl (2S,3R,αS)-2-deuterio-3-[N-benzyl-N-(α-methylbenzyl)amino]-3-(3'-fluorophenyl)propanoate(1332928-72-9)
EPA Substance Registry System: tert-butyl (2S,3R,αS)-2-deuterio-3-[N-benzyl-N-(α-methylbenzyl)amino]-3-(3'-fluorophenyl)propanoate(1332928-72-9)

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: 1332928-72-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1332928-72-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,2,9,2 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1332928-72:
(9*1)+(8*3)+(7*3)+(6*2)+(5*9)+(4*2)+(3*8)+(2*7)+(1*2)=159
159 % 10 = 9
So 1332928-72-9 is a valid CAS Registry Number.

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1332928-72-9Relevant academic research and scientific papers

Asymmetric synthesis of syn- and anti-α-deuterio-β3- phenylalanine derivatives

Davies, Stephen G.,Foster, Emma M.,McIntosh, Catherine R.,Roberts, Paul M.,Rosser, Timothy E.,Smith, Andrew D.,Thomson, James E.

experimental part, p. 1035 - 1050 (2011/10/04)

The conjugate addition of lithium (S)-N-benzyl-N-(α-methylbenzyl) amide to a range of aryl substituted tert-butyl cinnamate esters followed by reaction of the resultant lithium β-amino enolates with D2O provides access to anti configured α-deut

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