Cas 1173259-33-0,(3S,4S)-methyl 3-(allyldimethylsilyloxy)-2-bromo-4-(tert-butyldiphenylsilyloxy)-2-methylpentanoate

1173259-33-0

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Basic information

Product Name: (3S,4S)-methyl 3-(allyldimethylsilyloxy)-2-bromo-4-(tert-butyldiphenylsilyloxy)-2-methylpentanoate
Synonyms: (3S,4S)-methyl 3-(allyldimethylsilyloxy)-2-bromo-4-(tert-butyldiphenylsilyloxy)-2-methylpentanoate
CAS NO:1173259-33-0
Molecular Formula:
Molecular Weight: 577.706
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: (3S,4S)-methyl 3-(allyldimethylsilyloxy)-2-bromo-4-(tert-butyldiphenylsilyloxy)-2-methylpentanoate(CAS DataBase Reference)
NIST Chemistry Reference: (3S,4S)-methyl 3-(allyldimethylsilyloxy)-2-bromo-4-(tert-butyldiphenylsilyloxy)-2-methylpentanoate(1173259-33-0)
EPA Substance Registry System: (3S,4S)-methyl 3-(allyldimethylsilyloxy)-2-bromo-4-(tert-butyldiphenylsilyloxy)-2-methylpentanoate(1173259-33-0)

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: 1173259-33-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1173259-33-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,3,2,5 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1173259-33:
(9*1)+(8*1)+(7*7)+(6*3)+(5*2)+(4*5)+(3*9)+(2*3)+(1*3)=150
150 % 10 = 0
So 1173259-33-0 is a valid CAS Registry Number.

1173259-33-0Upstream product

4028-23-3 Allylchlorodimethylsilane

1173259-33-0Downstream Products

1173258-95-1 (R)-methyl 2-((1R,2S)-2-(tert-butyldiphenylsilyloxy)-1-hydroxypropyl)-2-methylpent-4-enoate

1173259-33-0Relevant academic research and scientific papers

Stereoselective quaternary center construction via atom-transfer radical cyclization using silicon tethers on acyclic precursors

Duplessis, Martin,Waltzy, Marie-Eve,Bencheqroun, Mohammed,Cardinal-David, Benoit,Guindon, Yvan

supporting information; experimental part, p. 3148 - 3151 (2009/12/07)

A novel strategy for the stereoselective construction of all-carbon quaternary centers on acyclic molecules using a two-step tandem process is reported. The first step involves an intramolecular and stereoselective atom transfer radical cyclization reacti

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