10271-44-0

Basic information

• Product Name: (3aalpha,4beta,5beta,7beta,7aalpha)-octahydro-4,7-methano-1H-inden-5-ol
• Synonyms: (3aalpha,4beta,5beta,7beta,7aalpha)-octahydro-4,7-methano-1H-inden-5-ol;2-Exo-hydroxy-exo-trimethylenenorbornane;3aα,4,5,6,7,7aα-Hexahydro-4β,7β-methanoindan-5α-ol;FKZJBAXKHJIQDU-IGORNWKESA-N
• CAS NO: 10271-44-0
• Molecular Formula: C₁₀H₁₆O
• Molecular Weight: 152.23344
• EINECS: 233-610-2
• Mol File: 10271-44-0.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 255.2°Cat760mmHg
• Flash Point: 105.5°C
• Appearance: /
• Density: 1.115g/cm³
• CAS DataBase Reference: (3aalpha,4beta,5beta,7beta,7aalpha)-octahydro-4,7-methano-1H-inden-5-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (3aalpha,4beta,5beta,7beta,7aalpha)-octahydro-4,7-methano-1H-inden-5-ol(10271-44-0)
• EPA Substance Registry System: (3aalpha,4beta,5beta,7beta,7aalpha)-octahydro-4,7-methano-1H-inden-5-ol(10271-44-0)

Safety Data

• Hazardous Substances Data: 10271-44-0(Hazardous Substances Data)

Usage

General Description

The chemical compound "(3aalpha,4beta,5beta,7beta,7aalpha)-octahydro-4,7-methano-1H-inden-5-ol" is a bicyclic sesquiterpene alcohol. It is a colorless, water-insoluble liquid with a sweet, woody odor. (3aalpha,4beta,5beta,7beta,7aalpha)-octahydro-4,7-methano-1H-inden-5-ol is commonly found in essential oils of various plants and is used in the fragrance and flavoring industries. It possesses anti-inflammatory and antimicrobial properties, and has been investigated for potential use in pharmaceuticals and cosmetics. Additionally, it has been shown to exhibit insecticidal and nematicidal activities, making it a potential candidate for use in agricultural applications.

Upstream product

• 1755-01-7 endo-Dicyclopentadien 
• 2825-83-4 (3aR,4R,7S,7aS)-octahydro-1H-4,7-methanoindene 
• 10271-45-1 (3aR^*,4S^*,5R^*,7S^*,7aR^*)-2,3,3a,4,5,6,7,7a-octahydro-5-hydroxy-4,7-methano-1H-indene 
• 31351-12-9 (3aR^*,4S^*,7S^*,7aR^*)-2,3,3a,4,5,6,7,7a-octahydro-4,7-methano-1H-inden-5-one 
• 10271-42-8 (3aRS,4SR,5SR,7SR,7aRS)-(±)-octahydro-1H-4,7-methanoinden-5-ol 
• 77-73-6 bi(cyclopentadiene) 
• 142-29-0 cyclopentene 
• 542-92-7 cyclopenta-1,3-diene 
• 7664-93-9 sulfuric acid 
• 2826-19-9 (3aR^*,4S^*,7R^*,7aS^*)-2,3,3a,4,7,7a-hexahydro-4,7-methano-1H-indene 
• 64-18-6 formic acid 
• 933-60-8 exo-dicyclopentadiene 
• 3385-61-3 exo-tricyclo<5.2.1.0^2,6>dec-3-en-exo-8-ol 
• 41498-15-1 (+/-)-5t-formyloxy-(3arH,7acH)-hexahydro-4t,7t-methano-indan 

Downstream Products

• 30983-74-5 (+/-)-5t-(4-nitro-benzoyloxy)-(3arH.7acH)-hexahydro-4c.7c-methano-indan 
• 30983-74-5 (3aRS,4RS,5RS,7RS,7aRS)-(±)-octahydro-1H-4,7-methanoinden-5-yl 4-nitrobenzoate 
• 1096687-70-5 (3aR,4R,5S,7R,7aR)-octahydro-1H-4,7-methanoinden-5-ol 
• 1096688-05-9 (3aS,4S,5R,7R,7aS)-octahydro-1H-4,7-methanoinden-5-ol 
• 10271-42-8 (1RS,2RS,6RS,7SR,8SR)-endo-tricyclo<5.2.1.0^2,6>deca-8-ol 
• 6319-15-9 (+/-)-(3ac,7ac)-octahydro-4r,7c-methano-inden-5-one oxime 
• 147588-02-1 (+/-)-6-oxo-5-(benzylidene-(ξ))-(3arH.7acH)-hexahydro-4t.7t-methano-indan 
• 75724-13-9 4-Nitro-benzoic acid (3aS,4S,5R,7S,7aS)-5-(3,5-bis-trifluoromethyl-phenyl)-octahydro-4,7-methano-inden-5-yl ester 
• 75724-13-9 4-Nitro-benzoic acid (3aR,4R,5R,7R,7aR)-5-(3,5-bis-trifluoromethyl-phenyl)-octahydro-4,7-methano-inden-5-yl ester 
• 75724-11-7 4-Nitro-benzoic acid (3aS,4S,5R,7S,7aS)-5-(4-trifluoromethyl-phenyl)-octahydro-4,7-methano-inden-5-yl ester 
• 75724-11-7 4-Nitro-benzoic acid (3aR,4R,5R,7R,7aR)-5-(4-trifluoromethyl-phenyl)-octahydro-4,7-methano-inden-5-yl ester 
• 75724-09-3 4-Nitro-benzoic acid (3aS,4S,5R,7S,7aS)-5-(3-trifluoromethyl-phenyl)-octahydro-4,7-methano-inden-5-yl ester 
• 75724-09-3 4-Nitro-benzoic acid (3aR,4R,5R,7R,7aR)-5-(3-trifluoromethyl-phenyl)-octahydro-4,7-methano-inden-5-yl ester 
• 75724-07-1 4-Nitro-benzoic acid (3aS,4S,5R,7S,7aS)-5-p-tolyl-octahydro-4,7-methano-inden-5-yl ester 

Relevant articles and documents

What Is the True Structure of D609, a Widely Used Lipid Related Enzyme Inhibitor?

(Chemical Equation Presented) D609 (1) has been used as a lipid-related enzyme inhibitor during the past three decades. Although it has eight possible stereoisomers, no systematic research considering its chirality has been performed. In this paper, eight possible chiral alcohols as direct precursors of D609 were synthesized, and their stereochemistries were elucidated by a vibrational circular dichroism (VCD) technique. Phosphatidylcholine-specific phospholipase C and sphingomyelin synthase inhibition assays of these isomers showed considerable differences in their activities.

Synthesis and Reactions of Tricyclic Monocarboxylic Acid Esters

A convenient and efficient method for preparing tricyclic esters has been developed on the basis of addition of C1-C3 monocarboxylic acids to tricyclo2,6>deca-3,8-diene and its dimethyl derivatives in the presence of p-toluenesulfonic acid.The orientation of the ester group in the products has been determined.Some reactions of the resulting esters have been studied, and their possible applications have been proposed.