Cas 913975-71-0,(+/-)-(E)-7-(4-methoxybenzyloxy)-3-(2,2,2-trimethyl-1,1-diphenyldisilyloxy)hept-4-enyl pivalate

913975-71-0

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Basic information

Product Name: (+/-)-(E)-7-(4-methoxybenzyloxy)-3-(2,2,2-trimethyl-1,1-diphenyldisilyloxy)hept-4-enyl pivalate
Synonyms: (+/-)-(E)-7-(4-methoxybenzyloxy)-3-(2,2,2-trimethyl-1,1-diphenyldisilyloxy)hept-4-enyl pivalate
CAS NO:913975-71-0
Molecular Formula:
Molecular Weight: 604.934
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: (+/-)-(E)-7-(4-methoxybenzyloxy)-3-(2,2,2-trimethyl-1,1-diphenyldisilyloxy)hept-4-enyl pivalate(CAS DataBase Reference)
NIST Chemistry Reference: (+/-)-(E)-7-(4-methoxybenzyloxy)-3-(2,2,2-trimethyl-1,1-diphenyldisilyloxy)hept-4-enyl pivalate(913975-71-0)
EPA Substance Registry System: (+/-)-(E)-7-(4-methoxybenzyloxy)-3-(2,2,2-trimethyl-1,1-diphenyldisilyloxy)hept-4-enyl pivalate(913975-71-0)

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: 913975-71-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 913975-71-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,3,9,7 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 913975-71:
(8*9)+(7*1)+(6*3)+(5*9)+(4*7)+(3*5)+(2*7)+(1*1)=200
200 % 10 = 0
So 913975-71-0 is a valid CAS Registry Number.

913975-71-0Upstream product

913975-71-0Downstream Products

913975-71-0Relevant academic research and scientific papers

Remote control of diastereoselectivity in intramolecular reactions of chiral allylsilanes

Judd, Weston R.,Ban, Sooho,Aube, Jeffrey

, p. 13736 - 13741 (2007/10/03)

During investigations of cyclization reactions between chiral allylsilanes and N-acyliminium ions, it was discovered that a suitably positioned benzyloxy group on the allylsilane component caused a reversal in the diastereoselectivity of these reactions r

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