Cas 271600-11-4,{(S)-1-[2-Oxo-2-((1R,2R,4R)-1,7,7-trimethyl-2-trimethylsilanyloxy-bicyclo[2.2.1]hept-2-yl)-ethyl]-butyl}-carbamic acid benzyl ester

271600-11-4

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Basic information

Product Name: {(S)-1-[2-Oxo-2-((1R,2R,4R)-1,7,7-trimethyl-2-trimethylsilanyloxy-bicyclo[2.2.1]hept-2-yl)-ethyl]-butyl}-carbamic acid benzyl ester
Synonyms: {(S)-1-[2-Oxo-2-((1R,2R,4R)-1,7,7-trimethyl-2-trimethylsilanyloxy-bicyclo[2.2.1]hept-2-yl)-ethyl]-butyl}-carbamic acid benzyl ester
CAS NO:271600-11-4
Molecular Formula:
Molecular Weight: 473.728
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: {(S)-1-[2-Oxo-2-((1R,2R,4R)-1,7,7-trimethyl-2-trimethylsilanyloxy-bicyclo[2.2.1]hept-2-yl)-ethyl]-butyl}-carbamic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: {(S)-1-[2-Oxo-2-((1R,2R,4R)-1,7,7-trimethyl-2-trimethylsilanyloxy-bicyclo[2.2.1]hept-2-yl)-ethyl]-butyl}-carbamic acid benzyl ester(271600-11-4)
EPA Substance Registry System: {(S)-1-[2-Oxo-2-((1R,2R,4R)-1,7,7-trimethyl-2-trimethylsilanyloxy-bicyclo[2.2.1]hept-2-yl)-ethyl]-butyl}-carbamic acid benzyl ester(271600-11-4)

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: 271600-11-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 271600-11-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,1,6,0 and 0 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 271600-11:
(8*2)+(7*7)+(6*1)+(5*6)+(4*0)+(3*0)+(2*1)+(1*1)=104
104 % 10 = 4
So 271600-11-4 is a valid CAS Registry Number.

271600-11-4Upstream product

271600-11-4Downstream Products

275816-76-7 Z-L-β-homonorvaline

271600-11-4Relevant academic research and scientific papers

α-Oxymethyl ketone enolates for the asymmetric Mannich reaction. From acetylene and N-alkoxycarbonylimines to β-amino acids

Palomo, Claudio,Oiarbide, Mikel,Gonzalez-Rego, M. Concepcion,Sharma, Arun K.,Garcia, Jesus M.,Gonzalez, Alberto,Landa, Cristina,Linden, Anthony

, p. 1063 - 1066 (2007/10/03)

The insufficient diastereoselectivity and generality, which are the main problems of the 'acetate' aza - aldol reaction, can now be addressed through the reaction of the lithium enolate of endo-O-trimethylsilyl acetyl isoborneol with various N[(p-tolylsul

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