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

1173258-95-1

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Basic information

Product Name: (R)-methyl 2-((1R,2S)-2-(tert-butyldiphenylsilyloxy)-1-hydroxypropyl)-2-methylpent-4-enoate
Synonyms: (R)-methyl 2-((1R,2S)-2-(tert-butyldiphenylsilyloxy)-1-hydroxypropyl)-2-methylpent-4-enoate
CAS NO:1173258-95-1
Molecular Formula:
Molecular Weight: 440.655
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: (R)-methyl 2-((1R,2S)-2-(tert-butyldiphenylsilyloxy)-1-hydroxypropyl)-2-methylpent-4-enoate(CAS DataBase Reference)
NIST Chemistry Reference: (R)-methyl 2-((1R,2S)-2-(tert-butyldiphenylsilyloxy)-1-hydroxypropyl)-2-methylpent-4-enoate(1173258-95-1)
EPA Substance Registry System: (R)-methyl 2-((1R,2S)-2-(tert-butyldiphenylsilyloxy)-1-hydroxypropyl)-2-methylpent-4-enoate(1173258-95-1)

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: 1173258-95-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1173258-95-1 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 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1173258-95:
(9*1)+(8*1)+(7*7)+(6*3)+(5*2)+(4*5)+(3*8)+(2*9)+(1*5)=161
161 % 10 = 1
So 1173258-95-1 is a valid CAS Registry Number.

1173258-95-1Upstream product

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

1173258-95-1Downstream Products

1173258-95-1Relevant 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

, p. 3148 - 3151 (2009)

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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