Cas 110510-90-2,tert-Butyl-((1R,3aS,4R,6R,8aS)-1-methoxy-6-phenylsulfanyl-1,2,3,3a,4,5,6,8a-octahydro-azulen-4-yloxy)-dimethyl-silane

110510-90-2

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Basic information

Product Name: tert-Butyl-((1R,3aS,4R,6R,8aS)-1-methoxy-6-phenylsulfanyl-1,2,3,3a,4,5,6,8a-octahydro-azulen-4-yloxy)-dimethyl-silane
Synonyms:
CAS NO:110510-90-2
Molecular Formula:
Molecular Weight: 404.689
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-((1R,3aS,4R,6R,8aS)-1-methoxy-6-phenylsulfanyl-1,2,3,3a,4,5,6,8a-octahydro-azulen-4-yloxy)-dimethyl-silane(CAS DataBase Reference)
NIST Chemistry Reference: tert-Butyl-((1R,3aS,4R,6R,8aS)-1-methoxy-6-phenylsulfanyl-1,2,3,3a,4,5,6,8a-octahydro-azulen-4-yloxy)-dimethyl-silane(110510-90-2)
EPA Substance Registry System: tert-Butyl-((1R,3aS,4R,6R,8aS)-1-methoxy-6-phenylsulfanyl-1,2,3,3a,4,5,6,8a-octahydro-azulen-4-yloxy)-dimethyl-silane(110510-90-2)

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: 110510-90-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 110510-90-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,5,1 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 110510-90:
(8*1)+(7*1)+(6*0)+(5*5)+(4*1)+(3*0)+(2*9)+(1*0)=62
62 % 10 = 2
So 110510-90-2 is a valid CAS Registry Number.

110510-90-2Upstream product

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110510-90-2Relevant academic research and scientific papers

A Synthetic Entry into the Ophiobolane Ring System

Rigby, James H.,Senanayake, Chrisantha

, p. 4634 - 4635 (1987)

A stereocontrolled construction of the angularly fused 5-8-5 ring system characteristic of the ophiobolin and ceroplastol sesterterpenes is reported.The synthesis is based on the elaboration of a cis-hydroazulene intermediate into the dicyclopenta cyclooctane system with control of relative stereochemistry at several critical centers.

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