146611-16-7

Basic information

• Product Name: 8β-hydroxy-9β-hydroxymethyl-(4α,4β),10β-trimethyl-(trans)-decahydronaphthalene
• CAS NO: 146611-16-7
• Molecular Weight: 226.359
• Mol File: 146611-16-7.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 8β-hydroxy-9β-hydroxymethyl-(4α,4β),10β-trimethyl-(trans)-decahydronaphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 8β-hydroxy-9β-hydroxymethyl-(4α,4β),10β-trimethyl-(trans)-decahydronaphthalene(146611-16-7)
• EPA Substance Registry System: 8β-hydroxy-9β-hydroxymethyl-(4α,4β),10β-trimethyl-(trans)-decahydronaphthalene(146611-16-7)

Safety Data

• Hazardous Substances Data: 146611-16-7(Hazardous Substances Data)

Upstream product

• 59633-89-5 3-oxo-5-(2,6,6-trimethyl-cyclohex-1-enyl)-pentanoic acid methyl ester 
• 17283-81-7 4-(2,6,6-Trimethyl-cyclohex-1-enyl)-butan-2-on 
• 56523-17-2 methyl 3-oxo-7,11-dimethyl-dodeca-6,10-dienoate 
• 65754-79-2 (+/-)-methyl (1β,2β,4aα,8aβ)-2-hydroxy-decahydro-5,5,8a-trimethylnaphthalene-1-carboxylate 
• 71712-61-3 (2Z,6E)-3-(Diethoxy-phosphoryloxy)-7,11-dimethyl-dodeca-2,6,10-trienoic acid methyl ester 
• 59684-77-4 (+/-)-8-oxo-12-nordriman-11-acid methyl ester 
• 65754-92-9 (+/-)-methyl (1β,2α,4aα,8aβ)-2-formyloxy-decahydro-5,5,8a-trimethylnaphthalene-1-carboxylate 
• 49749-46-4 1-methoxycarbonyl-2-oxo-1β,2,3,4,4aα,5,6,7,8aβ-octahydro-5,5,8a-trimethylnaphthalene 
• 65754-79-2 (+/-)-methyl (1α,2β,4aα,8aβ)-2-hydroxy-decahydro-5,5,8a-trimethylnaphthalene-1-carboxylate 
• 65754-79-2 (+/-)-methyl (1α,2α,4aα,8aβ)-2-hydroxy-decahydro-5,5,8a-trimethylnaphthalene-1-carboxylate 

Downstream Products

• 190451-39-9 (1R,2S,4aR,8aR)-2-hydroxy-decahydro-5,5,8a-trimethyl-1-naphthylmethanol 
• 301323-26-2 Acetic acid 5-methoxy-2-((3S,4aR,6aS,10aS,10bS)-7,7,10a-trimethyl-decahydro-naphtho[2,1-d][1,3]dioxin-3-yl)-phenyl ester 
• 564-20-5 norisoambreinolide 
• 10207-83-7 (+/-)-(1α,2β,4aβ,8aα)-decahydro-2-hydroxyl-2,5,5,8a-tetramethyl-1-naphthaleneethanol 
• 30801-12-8 methyl (5S,9S,10S,13E)-labda-8⁽¹⁷⁾,13-dien-15-oate 

Relevant articles and documents

A formal synthesis of (±)-Ambrox

Bicyclic diol 6, a direct precursor of (±)-Ambrox ((±)-7), has been synthesised in four steps (35% yield) from the known bicyclic enone 2.

Studies in lipase catalyzed transesterifications: Synthesis of (+)- albicanol, (+)-albicanyl acetate and chiral intermediates useful in the synthesis of drimanes and labdanes

Chiral intermediates [(-)-8, (+)-9, (-)-9, (+)-10, (-)-10, (+)-11] useful in the synthesis of drimanes and labdanes, as well as optically active albicanol 1 and albicanyl acetate 2, have been synthesized using enzymatic transesterification as the key step. (C) 2000 Elsevier Science Ltd.

Syntheses of 9β-(Hydroxymethyl)-4,4,10β-trimethyl-trans-decal-3β-ol

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