Cas 101032-68-2,(4RS,4aRS,5SR,7SR,8SR,8aSR)-4,5,7-trimethyl-8-(benzyloxy)-4-(hydroxymethyl)-3,4,4a,5,6,7,8,8a-octahydronaphthalene

101032-68-2

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Basic information

Product Name: (4RS,4aRS,5SR,7SR,8SR,8aSR)-4,5,7-trimethyl-8-(benzyloxy)-4-(hydroxymethyl)-3,4,4a,5,6,7,8,8a-octahydronaphthalene
Synonyms: (4RS,4aRS,5SR,7SR,8SR,8aSR)-4,5,7-trimethyl-8-(benzyloxy)-4-(hydroxymethyl)-3,4,4a,5,6,7,8,8a-octahydronaphthalene
CAS NO:101032-68-2
Molecular Formula:
Molecular Weight: 314.468
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: (4RS,4aRS,5SR,7SR,8SR,8aSR)-4,5,7-trimethyl-8-(benzyloxy)-4-(hydroxymethyl)-3,4,4a,5,6,7,8,8a-octahydronaphthalene(CAS DataBase Reference)
NIST Chemistry Reference: (4RS,4aRS,5SR,7SR,8SR,8aSR)-4,5,7-trimethyl-8-(benzyloxy)-4-(hydroxymethyl)-3,4,4a,5,6,7,8,8a-octahydronaphthalene(101032-68-2)
EPA Substance Registry System: (4RS,4aRS,5SR,7SR,8SR,8aSR)-4,5,7-trimethyl-8-(benzyloxy)-4-(hydroxymethyl)-3,4,4a,5,6,7,8,8a-octahydronaphthalene(101032-68-2)

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: 101032-68-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 101032-68-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,0,3 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 101032-68:
(8*1)+(7*0)+(6*1)+(5*0)+(4*3)+(3*2)+(2*6)+(1*8)=52
52 % 10 = 2
So 101032-68-2 is a valid CAS Registry Number.

101032-68-2Upstream product

101032-68-2Downstream Products

101032-66-0 (4RS,4aRS,5SR,7SR,8SR,8aSR)-4,5,7-trimethyl-8-(benzyloxy)-3,4,4a,5,6,7,8,8a-octahydronaphthalene-4-carboxaldehyde

101032-68-2Relevant academic research and scientific papers

Acyclic Stereocontrol in Catalyzed Intramolecular Diels-Alder Cyclizations of 4-Methyl-2,8,10-undecatrienals

Marshall, James A.,Audia, James E.,Grote, Jonathan

, p. 1155 - 1157 (1986)

A 4-methyl substituent has been found to exert profound diastereocontrol on the Diels-Alder cyclization of 2,8,10-undecatrienals in the presence of ethylaluminum dichloride, giving trans-fused 5-methyl-3,4,4a,5,6,7,8,8a-octahydronaphthalene-4-carboxaldehy

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