Cas 197231-58-6,[(1S,2S)-2,3-Bis-(tert-butyl-dimethyl-silanyloxy)-1-phenethyl-propyl]-carbamic acid tert-butyl ester

197231-58-6

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Basic information

Product Name: [(1S,2S)-2,3-Bis-(tert-butyl-dimethyl-silanyloxy)-1-phenethyl-propyl]-carbamic acid tert-butyl ester
Synonyms: [(1S,2S)-2,3-Bis-(tert-butyl-dimethyl-silanyloxy)-1-phenethyl-propyl]-carbamic acid tert-butyl ester
CAS NO:197231-58-6
Molecular Formula:
Molecular Weight: 523.904
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: [(1S,2S)-2,3-Bis-(tert-butyl-dimethyl-silanyloxy)-1-phenethyl-propyl]-carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [(1S,2S)-2,3-Bis-(tert-butyl-dimethyl-silanyloxy)-1-phenethyl-propyl]-carbamic acid tert-butyl ester(197231-58-6)
EPA Substance Registry System: [(1S,2S)-2,3-Bis-(tert-butyl-dimethyl-silanyloxy)-1-phenethyl-propyl]-carbamic acid tert-butyl ester(197231-58-6)

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: 197231-58-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 197231-58-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,7,2,3 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 197231-58:
(8*1)+(7*9)+(6*7)+(5*2)+(4*3)+(3*1)+(2*5)+(1*8)=156
156 % 10 = 6
So 197231-58-6 is a valid CAS Registry Number.

197231-58-6Upstream product

197231-58-6Downstream Products

197231-58-6Relevant academic research and scientific papers

Enantioselective synthesis of (S)-Vigabatrin

Alcon, Montserrat,Poch, Marta,Moyano, Albert,Pericas, Miquel A.,Riera, Antoni

, p. 2967 - 2974 (2007/10/03)

An asymmetric synthesis of fully protected (S)-Vigabatrin has been developed. The key intermediate in the sequence is enantiomerically pure N-Boc-5-phenyl-3-amino-1,2-diol 5a, obtained from (E)-5-phenyl-2-penten-1-ol by employing a catalytic Sharpless epo

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