110557-39-6

Basic information

• Product Name: 1,4-Naphthalenediol,1,4,4a,5,6,7,8,8a-octahydro-1-(hydroxymethyl)-2,5,5,8a-tetramethyl-,(1R,4S,4aS,8aS)-
• Synonyms: 1,4-Naphthalenediol,1,4,4a,5,6,7,8,8a-octahydro-1-(hydroxymethyl)-2,5,5,8a-tetramethyl-, [1R-(1a,4a,4aa,8ab)]-; Albrassitriol
• CAS NO: 110557-39-6
• Molecular Formula: C15H26 O3
• Molecular Weight: 254.37
• Mol File: 110557-39-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1,4-Naphthalenediol,1,4,4a,5,6,7,8,8a-octahydro-1-(hydroxymethyl)-2,5,5,8a-tetramethyl-,(1R,4S,4aS,8aS)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-Naphthalenediol,1,4,4a,5,6,7,8,8a-octahydro-1-(hydroxymethyl)-2,5,5,8a-tetramethyl-,(1R,4S,4aS,8aS)-(110557-39-6)
• EPA Substance Registry System: 1,4-Naphthalenediol,1,4,4a,5,6,7,8,8a-octahydro-1-(hydroxymethyl)-2,5,5,8a-tetramethyl-,(1R,4S,4aS,8aS)-(110557-39-6)

Safety Data

• Hazardous Substances Data: 110557-39-6(Hazardous Substances Data)

Usage

Chemical structure

A complex and specific structure containing a naphthalenediol group, a tetramethyl group, and a hydroxymethyl group.

Stereochemistry

The compound's stereochemistry is denoted by the (1R,4S,4aS,8aS) classification, which indicates the spatial arrangement of its atoms.

Potential applications

The compound may have potential applications in various fields such as pharmaceuticals, agrochemicals, or materials science.

Further investigation

The precise uses and properties of the compound would require further investigation and analysis to fully understand its potential and limitations.
Please note that this list is based on the limited information provided in the material and may not be exhaustive. Further research and analysis would be necessary to fully understand the properties and potential applications of this compound.

Upstream product

• 110547-82-5 ((1S,4aS,8aR)-2,5,5,8a-Tetramethyl-4-oxo-1,4,4a,5,6,7,8,8a-octahydronaphthalen-1-yl)methyl acetate 
• 127681-57-6 (4aS,8aS)-3,4a,8,8-Tetramethyl-4-methylene-4a,5,6,7,8,8a-hexahydronaphthalen-1(4H)-one 
• 127681-58-7 (4R,4aS,8aS)-4-Hydroxy-4-(hydroxymethyl)-3,4a,8,8-tetramethyl-4a,5,6,7,8,8a-hexahydronaphthalen-1(4H)-one 
• 326795-16-8 (1S,3R,4R,4aS,8aS)-3-(Acetyloxy)-4-formyl-3,4a,8,8-tetramethyldecahydronaphthalen-1-yl acetate 
• 326795-27-1 (1S,4aS,8aS)-4-(Hydroxymethyl)-3,4a,8,8-tetramethyl-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl acetate 
• 326795-17-9 (1S,4aS,8S)-4-Formyl-3,4a,8,8-tetramethyl-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl acetate 
• 326795-28-2 Acetic acid (1aR,3S,3aS,7aS,7bR)-7b-hydroxymethyl-1a,4,4,7a-tetramethyl-decahydro-1-oxa-cyclopropa[a]naphthalen-3-yl ester 
• 326795-30-6 (1S,3R,4S,4aR,8aS)-4-({[tert-Butyl(dimethyl)silyl]oxy}methyl)-3,4a,8,8-tetramethyldecahydronaphthalene-1,3-diol 
• 326795-31-7 (3R,4S,4aR,8aS)-4-({[tert-Butyl(dimethyl)silyl]oxy}methyl)-3-hydroxy-3,4a,8,8-tetramethyloctahydronaphthalen-1(2H)-one 
• 127681-59-8 (4S,4aR,8aS)-4-({[tert-Butyl(dimethyl)silyl]oxy}methyl)-3,4a,8,8-tetramethyl-4a,5,6,7,8,8a-hexahydronaphthalen-1(4H)-one 
• 326795-29-3 (1S,3R,4S,4aS,8aS)-4-(Hydroxymethyl)-3,4a,8,8-tetramethyldecahydronaphthalene-1,3-diol 
• 74635-87-3 (4S,4aR,8aS)-4-(Hydroxymethyl)-3,4a,8,8-tetramethyl-4a,5,6,7,8,8a-hexahydronaphthalen-1(4H)-one 

Relevant articles and documents

Synthesis of drimanes from (+)-larixol

The selective transformation of the side chain of larixol 1 to a functionalized one-carbon moiety leads to 6,8-diacetoxydrimenal 13, which was converted to the drimanes (-)-albrassitriol (2), (-)-drimenol (3), (-)-uvidin C (4) and (-)-epi-albrassitriol (5).