3385-61-3

Basic information

• Product Name: 3a,4,5,6,7,7a-hexahydro-4,7-methano-1H-inden-6-ol
• Synonyms: 3a,4,5,6,7,7a-hexahydro-4,7-methano-1H-inden-6-ol;3A,4,5,6,7,7A-Hexahydro-4,7-methanoinden-6-ol;4,7-Methano-1H-inden-6-ol, 3A,4,5,6,7,7A-hexahydro-;Einecs 222-197-4;Tricyclo(5.2.1.02,6)dec-3-en-8-ol;3A,4,5,6,7,7A-HEXAHYDRO-3H-4,7-METHANO-INDEN-5-OL
• CAS NO: 3385-61-3
• Molecular Formula: C₁₀H₁₄O
• Molecular Weight: 150.21756
• EINECS: 222-197-4
• Mol File: 3385-61-3.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 245.9°Cat760mmHg
• Flash Point: 90.2°C
• Appearance: /
• Density: 1.157g/cm³
• Vapor Pressure: 0.00462mmHg at 25°C
• Refractive Index: 1.583
• CAS DataBase Reference: 3a,4,5,6,7,7a-hexahydro-4,7-methano-1H-inden-6-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 3a,4,5,6,7,7a-hexahydro-4,7-methano-1H-inden-6-ol(3385-61-3)
• EPA Substance Registry System: 3a,4,5,6,7,7a-hexahydro-4,7-methano-1H-inden-6-ol(3385-61-3)

Safety Data

• Hazardous Substances Data: 3385-61-3(Hazardous Substances Data)

Usage

General Description

3a,4,5,6,7,7a-hexahydro-4,7-methano-1H-inden-6-ol, also known as hexahydro-4,7-methanoindene-6-ol, is a chemical compound with a complex molecular structure. It is a saturated bicyclic compound containing a six-membered ring fused to a five-membered ring with a hydroxyl group attached. 3a,4,5,6,7,7a-hexahydro-4,7-methano-1H-inden-6-ol is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It has also been shown to exhibit antioxidant and anti-inflammatory properties, making it of interest for potential medicinal applications. Additionally, it has been used in the fragrance industry to produce sweet, floral, and woody scents in perfumes and personal care products.

InChI:InChI=1/C10H14O/c11-10-5-6-4-9(10)8-3-1-2-7(6)8/h1-2,6-11H,3-5H2

Upstream product

• 64-18-6 formic acid 
• 933-60-8 exo-dicyclopentadiene 
• 1755-01-7 endo-Dicyclopentadien 
• 77-73-6 bi(cyclopentadiene) 

Downstream Products

• 13380-94-4 octahydro-4,7-methano-inden-5-one 
• 14888-58-5 (1RS,2SR,6RS,7RS)tricyclo[5.2.1.02,6]dec-3-en-8-on 
• 10271-42-8 Octahydro-endo-4,7-methanoinden-endo-5-ol 
• 13380-89-7 tricyclo[5.2.1.02,6 ]deca-8-yl alcohol 

Relevant articles and documents

Method of preparing tricyclic decenol, reaction intermediate and preparation method of reaction intermediate

The invention relates to a method of preparing tricyclic decenol, a reaction intermediate and a preparation method of the reaction intermediate. The preparation method of tricyclic decenol comprises the steps of allowing dicyclopentadiene and trifluoroacetic acid to give an addition reaction to form tricyclodecenyl trifluoroacetate, and performing hydrolysis through potassium carbonate to form tricyclic decenol. The preparation method is low in reaction temperature, short in time, and environmentally friendly; the quantity of reaction pollutants is small; a yield of a tricyclic decenol productcan reach 94%; and at the same time, the purity of tricyclic decenol can reach 98%.

Enantioselectivity in odor perception synthesis and olfactory properties of the new tricyclic sandalwood odorant Fleursandol

The 3-methyl-4-(tricyclo[5.2.1.02,6]dec-4-en-8-ylidene)butan-2- ols (=Fleursandol; rac-10), a new class of sandalwood odorants, were synthesized in their enantiomerically pure forms by use of tricyclo[5.2.1.0 2,6]dec-4-en-8-ones 17 and ent-17 and (tetrahydro-2H-pyran-2-yl)- protected 4-bromo-3-methylbutan-2-ols 22 and ent-22 as starting materials (Schemes 2-4). Only four of 16 possible stereoisomers of rac-10 possess the typical, very pleasant, long-lasting sandalwood odor (Table 1). The (2S,3R,4E,1′R,2′R,6′R,7′R)-isomer ent-10a is by far the most important representative, with an odor threshold of 5 μg/l in H 2O.

Vapor-phase Hydration of Dicyclopentadiene Catalyzed by Niobic Acid

Vapor-phase hydration of dicyclopentadiene in a flow system was promoted by niobic acid.Maximum conversion to the hydrated product was obtained at around the boiling point of dicyclopentadiene, 170 deg C.Niobic acid rapidly decreased its catalytic activity when it was heat-treated at temperatures higher than 300 deg C.