Cas 958887-75-7,(1S)-[5-(tert-butyldimethylsilanyloxy)-1-methyl-8-oxo-tetradec-3-enyl]carbamic acid benzyl ester

958887-75-7

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Basic information

Product Name: (1S)-[5-(tert-butyldimethylsilanyloxy)-1-methyl-8-oxo-tetradec-3-enyl]carbamic acid benzyl ester
Synonyms: (1S)-[5-(tert-butyldimethylsilanyloxy)-1-methyl-8-oxo-tetradec-3-enyl]carbamic acid benzyl ester
CAS NO:958887-75-7
Molecular Formula:
Molecular Weight: 503.798
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)-[5-(tert-butyldimethylsilanyloxy)-1-methyl-8-oxo-tetradec-3-enyl]carbamic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (1S)-[5-(tert-butyldimethylsilanyloxy)-1-methyl-8-oxo-tetradec-3-enyl]carbamic acid benzyl ester(958887-75-7)
EPA Substance Registry System: (1S)-[5-(tert-butyldimethylsilanyloxy)-1-methyl-8-oxo-tetradec-3-enyl]carbamic acid benzyl ester(958887-75-7)

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: 958887-75-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 958887-75-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,8,8,8 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 958887-75:
(8*9)+(7*5)+(6*8)+(5*8)+(4*8)+(3*7)+(2*7)+(1*5)=267
267 % 10 = 7
So 958887-75-7 is a valid CAS Registry Number.

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958887-75-7Relevant academic research and scientific papers

Diastereoselective synthesis of 2,6-trans-disubstituted piperidines via sequential cross-metathesis-cationic cyclisation

Mix, Stefan,Blechert, Siegfried

, p. 157 - 160 (2008/02/03)

Ruthenium-catalysed cross-metathesis of protected homoallylamine derivatives with vinyl carbinols furnished allylic alcohols, which underwent stereoconvergent cyclisation to trans-tetrahydropyridines upon treatment with BF3-OEt2. The

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