Cas 132150-06-2,(2R,3S)-6-(tert-Butyl-dimethyl-silanyloxy)-1-(tert-butyl-diphenyl-silanyloxy)-3-methyl-non-4-yn-2-ol

132150-06-2

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Basic information

Product Name: (2R,3S)-6-(tert-Butyl-dimethyl-silanyloxy)-1-(tert-butyl-diphenyl-silanyloxy)-3-methyl-non-4-yn-2-ol
Synonyms:
CAS NO:132150-06-2
Molecular Formula:
Molecular Weight: 538.918
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: (2R,3S)-6-(tert-Butyl-dimethyl-silanyloxy)-1-(tert-butyl-diphenyl-silanyloxy)-3-methyl-non-4-yn-2-ol(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3S)-6-(tert-Butyl-dimethyl-silanyloxy)-1-(tert-butyl-diphenyl-silanyloxy)-3-methyl-non-4-yn-2-ol(132150-06-2)
EPA Substance Registry System: (2R,3S)-6-(tert-Butyl-dimethyl-silanyloxy)-1-(tert-butyl-diphenyl-silanyloxy)-3-methyl-non-4-yn-2-ol(132150-06-2)

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: 132150-06-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 132150-06-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,1,5 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 132150-06:
(8*1)+(7*3)+(6*2)+(5*1)+(4*5)+(3*0)+(2*0)+(1*6)=72
72 % 10 = 2
So 132150-06-2 is a valid CAS Registry Number.

132150-06-2Upstream product

132150-06-2Downstream Products

132150-06-2Relevant academic research and scientific papers

The opening of trans-2-3-epoxy-1-butanol derivatives with organometallic reagents

Skrydstrup, Troels,Benechie, Michel,Khuong-Huu, Francoise

, p. 7145 - 7148 (2007/10/02)

The opening of trans-2-3-epoxy-butan-1-ol derivatives with various organometallic reagents was studied to find the best conditions necessary to obtain convenient yields and regioselectivities for their application in natural product synthesis.

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