95263-32-4

Basic information

• Product Name: (11aR)-1,1-dimethyl-8-(propan-2-yl)-1,2,3,4,5,10,11,11a-octahydro-4aH-dibenzo[a,d][7]annulene-4a,5,7-triol
• CAS NO: 95263-32-4
• Molecular Formula: C₂₀H₃₀O₃
• Molecular Weight: 318.4504
• Mol File: 95263-32-4.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 455.8°C at 760 mmHg
• Flash Point: 204.4°C
• Density: 1.13g/cm³
• Vapor Pressure: 4.22E-09mmHg at 25°C
• Refractive Index: 1.571
• CAS DataBase Reference: (11aR)-1,1-dimethyl-8-(propan-2-yl)-1,2,3,4,5,10,11,11a-octahydro-4aH-dibenzo[a,d][7]annulene-4a,5,7-triol(CAS DataBase Reference)
• NIST Chemistry Reference: (11aR)-1,1-dimethyl-8-(propan-2-yl)-1,2,3,4,5,10,11,11a-octahydro-4aH-dibenzo[a,d][7]annulene-4a,5,7-triol(95263-32-4)
• EPA Substance Registry System: (11aR)-1,1-dimethyl-8-(propan-2-yl)-1,2,3,4,5,10,11,11a-octahydro-4aH-dibenzo[a,d][7]annulene-4a,5,7-triol(95263-32-4)

Safety Data

• Hazardous Substances Data: 95263-32-4(Hazardous Substances Data)

Usage

Description

(11aR)-1,1-dimethyl-8-(propan-2-yl)-1,2,3,4,5,10,11,11a-octahydro-4aH-dibenzo[a,d][7]annulene-4a,5,7-triol is a complex chemical compound that features a cyclic structure with two fused benzene rings. It is a triol, characterized by the presence of three hydroxyl (OH) groups, and also contains a tertiary alcohol group. This unique arrangement of functional groups and its cyclic nature may endow it with special properties, making it a candidate for exploration in medicinal chemistry and pharmaceutical applications. However, further research is required to fully understand its characteristics and potential uses.

Uses

Used in Medicinal Chemistry:
(11aR)-1,1-dimethyl-8-(propan-2-yl)-1,2,3,4,5,10,11,11a-octahydro-4aH-dibenzo[a,d][7]annulene-4a,5,7-triol is used as a compound of interest in medicinal chemistry for its potential to interact with biological targets due to its hydroxyl groups and cyclic structure. The presence of multiple hydroxyl groups may allow for hydrogen bonding, which is crucial for molecular recognition and binding processes.
Used in Pharmaceutical Development:
In the pharmaceutical industry, (11aR)-1,1-dimethyl-8-(propan-2-yl)-1,2,3,4,5,10,11,11a-octahydro-4aH-dibenzo[a,d][7]annulene-4a,5,7-triol may be utilized as a starting material or a structural component in the design of new drugs. Its unique structural features could be leveraged to create molecules with specific therapeutic effects, targeting a range of diseases or conditions.

Upstream product

• 99152-21-3 (4aR,11aS)-4a,7-Dihydroxy-8-isopropyl-1,1-dimethyl-1,2,3,4,4a,10,11,11a-octahydro-dibenzo[a,d]cyclohepten-5-one 

Downstream Products

• 95263-39-1 4-Bromo-benzoic acid (5S,5aR,9aS)-5,5a-dihydroxy-2-isopropyl-9,9-dimethyl-5a,6,7,8,9,9a,10,11-octahydro-5H-dibenzo[a,d]cyclohepten-3-yl ester 
• 95263-38-0 C₃₄H₃₆Br₂O₅ 
• 106540-57-2 2-[2-((S)-2,2-Dimethyl-6-oxo-cyclohexyl)-ethyl]-4-isopropyl-5-methoxy-benzoic acid methyl ester 
• 106540-56-1 (S)-2-[2-(2-Hydroxymethyl-5-isopropyl-4-methoxy-phenyl)-ethyl]-3,3-dimethyl-cyclohexanol 
• 99152-14-4 (+)-pisiferanol 
• 76210-23-6 pisiferin 
• 95263-36-8 2-[2-((S)-2,2-Dimethyl-6-oxo-cyclohexyl)-ethyl]-4-isopropyl-5-methoxy-benzoic acid 
• 95263-35-7 2-[2-((S)-2,2-Dimethyl-6-oxo-cyclohexyl)-ethyl]-4-isopropyl-5-methoxy-benzaldehyde 

Relevant articles and documents

TERPENOIDS FROM THE SEED OF CHAMAECYPARIS PISIFERA: THE STRUCTURES OF SIX DITERPENOIDS

Key Word Index - Chamaecyparis pisifera; Cupressaceae; chemotaxonomy; mono-, sesqui- and diterpenes; 20-nor-abietane; 9(10 -> 20)-abeo-abietane. - Six new diterpenes, 12-hydroxy-20-nor-abieta-1(10),2,8,11,13-pentaene, pisiferanol (10S,12-dihydroxy-9(10 -> 20)-abeo-abieta-8,11,13-triene), pisiferadinol (20S-hydroxypisiferanol), 12-deoxypisiferanol, 1β-hydroxyisopisiferin (1R,12-dihydroxy-9(10 -> 20)-abeo-abieta-8,10(20),11,13-tetraene), and the dimethylamine salt of O-methylpisiferic acid were isolated from the seed of Chamaecyparis pisifera.The structures of these diterpenes were established by spectral and chemical methods.In addition, 15 mono-, four sesqui- and nine diterpenes were identified.