Cas 1190597-36-4,(3-((3E,7E)-10-((S)-3,3-dimethyloxiran-2-yl)-4,8-dimethyldeca-3,7-dienyl)-2-methoxy-4-methylphenoxy)triisopropylsilane

1190597-36-4

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Basic information

Product Name: (3-((3E,7E)-10-((S)-3,3-dimethyloxiran-2-yl)-4,8-dimethyldeca-3,7-dienyl)-2-methoxy-4-methylphenoxy)triisopropylsilane
Synonyms: (3-((3E,7E)-10-((S)-3,3-dimethyloxiran-2-yl)-4,8-dimethyldeca-3,7-dienyl)-2-methoxy-4-methylphenoxy)triisopropylsilane
CAS NO:1190597-36-4
Molecular Formula:
Molecular Weight: 528.891
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: (3-((3E,7E)-10-((S)-3,3-dimethyloxiran-2-yl)-4,8-dimethyldeca-3,7-dienyl)-2-methoxy-4-methylphenoxy)triisopropylsilane(CAS DataBase Reference)
NIST Chemistry Reference: (3-((3E,7E)-10-((S)-3,3-dimethyloxiran-2-yl)-4,8-dimethyldeca-3,7-dienyl)-2-methoxy-4-methylphenoxy)triisopropylsilane(1190597-36-4)
EPA Substance Registry System: (3-((3E,7E)-10-((S)-3,3-dimethyloxiran-2-yl)-4,8-dimethyldeca-3,7-dienyl)-2-methoxy-4-methylphenoxy)triisopropylsilane(1190597-36-4)

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: 1190597-36-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1190597-36-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,0,5,9 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1190597-36:
(9*1)+(8*1)+(7*9)+(6*0)+(5*5)+(4*9)+(3*7)+(2*3)+(1*6)=174
174 % 10 = 4
So 1190597-36-4 is a valid CAS Registry Number.

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1190597-36-4Relevant academic research and scientific papers

A short enantioselective total synthesis of the fundamental pentacyclic triterpene lupeol

Surendra, Karavadhi,Corey

, p. 13928 - 13929 (2009)

(Chemical Equation Presented) The first enantioselective synthesis of lupeol has been developed by applying two carefully crafted cation-π cyclization stages to generate the pentacyclic structure with complete stereocontrol. The synthesis (Scheme 1) is no

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