Cas 104461-71-4,(1R,4aS,8aR)-1-(1,2,4a,5,6,7,8,8a-Octahydro-naphthalen-1-yl)-methanol

104461-71-4

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Basic information

Product Name: (1R,4aS,8aR)-1-(1,2,4a,5,6,7,8,8a-Octahydro-naphthalen-1-yl)-methanol
Synonyms:
CAS NO:104461-71-4
Molecular Formula:
Molecular Weight: 166.263
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: (1R,4aS,8aR)-1-(1,2,4a,5,6,7,8,8a-Octahydro-naphthalen-1-yl)-methanol(CAS DataBase Reference)
NIST Chemistry Reference: (1R,4aS,8aR)-1-(1,2,4a,5,6,7,8,8a-Octahydro-naphthalen-1-yl)-methanol(104461-71-4)
EPA Substance Registry System: (1R,4aS,8aR)-1-(1,2,4a,5,6,7,8,8a-Octahydro-naphthalen-1-yl)-methanol(104461-71-4)

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: 104461-71-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 104461-71-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,4,6 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 104461-71:
(8*1)+(7*0)+(6*4)+(5*4)+(4*6)+(3*1)+(2*7)+(1*1)=94
94 % 10 = 4
So 104461-71-4 is a valid CAS Registry Number.

104461-71-4Upstream product

104461-67-8 ((1S,5R,7R)-10,10-Dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-(1R,4aS,8aR)-1,2,4a,5,6,7,8,8a-octahydro-naphthalen-1-yl-methanone

104461-71-4Downstream Products

104461-71-4Relevant academic research and scientific papers

ASYMMETRIC INTRAMOLECULAR DIELS-ALDER REACTIONS OF N-ACYL-CAMPHOR-SULTAM TRIENES.

Oppolzer, Wolfgang,Dupuis, Dominique

, p. 5437 - 5440 (1985)

Treatment of triene-imides 4 with EtAlCl2 at -20 deg C gave crystalline cycloadducts 5 which furnished enantiomerically pure bicyclic alcohols 9 with regeneration of the chiral auxilary.

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