Cas 1217870-00-2,tert-butyl[(3R,4R,5R,6S)-5-methoxy-1-(4-methoxybenzyloxy)-4,6,9-trimethyldec-8-en-3-yloxy]dimethylsilane

1217870-00-2

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Basic information

Product Name: tert-butyl[(3R,4R,5R,6S)-5-methoxy-1-(4-methoxybenzyloxy)-4,6,9-trimethyldec-8-en-3-yloxy]dimethylsilane
Synonyms: tert-butyl[(3R,4R,5R,6S)-5-methoxy-1-(4-methoxybenzyloxy)-4,6,9-trimethyldec-8-en-3-yloxy]dimethylsilane
CAS NO:1217870-00-2
Molecular Formula:
Molecular Weight: 478.788
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: tert-butyl[(3R,4R,5R,6S)-5-methoxy-1-(4-methoxybenzyloxy)-4,6,9-trimethyldec-8-en-3-yloxy]dimethylsilane(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl[(3R,4R,5R,6S)-5-methoxy-1-(4-methoxybenzyloxy)-4,6,9-trimethyldec-8-en-3-yloxy]dimethylsilane(1217870-00-2)
EPA Substance Registry System: tert-butyl[(3R,4R,5R,6S)-5-methoxy-1-(4-methoxybenzyloxy)-4,6,9-trimethyldec-8-en-3-yloxy]dimethylsilane(1217870-00-2)

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: 1217870-00-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1217870-00-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,7,8,7 and 0 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1217870-00:
(9*1)+(8*2)+(7*1)+(6*7)+(5*8)+(4*7)+(3*0)+(2*0)+(1*0)=142
142 % 10 = 2
So 1217870-00-2 is a valid CAS Registry Number.

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1217870-00-2Relevant academic research and scientific papers

Total synthesis of gem-difluoromethylenated analogues of pironetin

Lin, Jing,Qing, Feng-Ling,Yue, Xuyi,Huang, Peng,Cui, Daxiang

experimental part, p. 267 - 275 (2010/04/02)

The straightforward synthesis of four gem-difluoromethylenated analogues of pironetin is described. Our synthesis features the efficient construction of the key intermediates through the indium--mediated gem-difluoropropargylation of aldehydes with the fl

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