Cas 1392437-91-0,butyl (2S,6S,E)-2-{benzyloxycarbonyl[(1R)-(1-phenylethyl)]-amino}-6-(tert-butyldimethylsilyloxy)hept-4-enoate

1392437-91-0

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Basic information

Product Name: butyl (2S,6S,E)-2-{benzyloxycarbonyl[(1R)-(1-phenylethyl)]-amino}-6-(tert-butyldimethylsilyloxy)hept-4-enoate
Synonyms: butyl (2S,6S,E)-2-{benzyloxycarbonyl[(1R)-(1-phenylethyl)]-amino}-6-(tert-butyldimethylsilyloxy)hept-4-enoate
CAS NO:1392437-91-0
Molecular Formula:
Molecular Weight: 567.841
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: butyl (2S,6S,E)-2-{benzyloxycarbonyl[(1R)-(1-phenylethyl)]-amino}-6-(tert-butyldimethylsilyloxy)hept-4-enoate(CAS DataBase Reference)
NIST Chemistry Reference: butyl (2S,6S,E)-2-{benzyloxycarbonyl[(1R)-(1-phenylethyl)]-amino}-6-(tert-butyldimethylsilyloxy)hept-4-enoate(1392437-91-0)
EPA Substance Registry System: butyl (2S,6S,E)-2-{benzyloxycarbonyl[(1R)-(1-phenylethyl)]-amino}-6-(tert-butyldimethylsilyloxy)hept-4-enoate(1392437-91-0)

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: 1392437-91-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1392437-91-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,2,4,3 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1392437-91:
(9*1)+(8*3)+(7*9)+(6*2)+(5*4)+(4*3)+(3*7)+(2*9)+(1*1)=180
180 % 10 = 0
So 1392437-91-0 is a valid CAS Registry Number.

1392437-91-0Upstream product

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1392437-91-0Relevant academic research and scientific papers

Remote stereocontrol in reactions between 4- and 5-alkoxyalk-2- enylstannanes and 1-alkoxycarbonylimines and analogues: Stereoselective approaches to novel α-amino acids

Hallett, David J.,Tanikkul, Nongluk,Thomas, Eric J.

supporting information; experimental part, p. 6130 - 6158 (2012/09/05)

Reactions of the allyltin trichloride 45 generated from (4S)-4-benzyloxypent-2-enyl(tributyl)stannane 1 with imines prepared from glyoxylates proceed with useful levels of 1,5-stereocontrol in favour of (4E)-2,6-anti-2-(alkylamino)-6-benzyloxyhept-4-enoat

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