38748-96-8

Basic information

• Product Name: (1alpha,3alpha,4beta,6alpha)-4,7,7-trimethylbicyclo[4.1.0]heptan-3-ol
• Synonyms: (1alpha,3alpha,4beta,6alpha)-4,7,7-trimethylbicyclo[4.1.0]heptan-3-ol
• CAS NO: 38748-96-8
• Molecular Formula: C₁₀H₁₈O
• Molecular Weight: 154.24932
• EINECS: 254-114-2
• Mol File: 38748-96-8.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 210.6°Cat760mmHg
• Flash Point: 84.4°C
• Appearance: /
• Density: 0.96g/cm³
• Refractive Index: 1.484
• CAS DataBase Reference: (1alpha,3alpha,4beta,6alpha)-4,7,7-trimethylbicyclo[4.1.0]heptan-3-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (1alpha,3alpha,4beta,6alpha)-4,7,7-trimethylbicyclo[4.1.0]heptan-3-ol(38748-96-8)
• EPA Substance Registry System: (1alpha,3alpha,4beta,6alpha)-4,7,7-trimethylbicyclo[4.1.0]heptan-3-ol(38748-96-8)

Safety Data

• Hazardous Substances Data: 38748-96-8(Hazardous Substances Data)

Usage

General Description

The chemical (1alpha,3alpha,4beta,6alpha)-4,7,7-trimethylbicyclo[4.1.0]heptan-3-ol, also known as tricyclo[4.1.0.0(3,6)]heptan-3-ol, is a bicyclic terpene alcohol compound. It is a colorless liquid with a sweet and woody odor, and it is commonly found in various essential oils, including those of conifers and citrus fruits. This chemical is often used in the fragrance and flavor industries, as it contributes to the pleasant aroma and taste of many natural products. Additionally, it has been studied for its potential pharmacological properties, such as its antibacterial and anti-inflammatory effects. Overall, (1alpha,3alpha,4beta,6alpha)-4,7,7-trimethylbicyclo[4.1.0]heptan-3-ol is a versatile compound with a variety of applications in different fields.

InChI:InChI=1/C10H18O/c1-6-4-7-8(5-9(6)11)10(7,2)3/h6-9,11H,4-5H2,1-3H3/t6-,7+,8-,9-/m0/s1

Upstream product

• 5208-43-5 (1R,3R,4R,6S)-4,7,7-trimethylbicyclo[4.1.0]hept-3-yl 4-methylbenzenesulfonate 
• 13466-78-9 3-carene 
• 64-17-5 ethanol 
• 4176-01-6 (-)-isocaranone 
• 60-29-7 diethyl ether 
• 936-92-5 (1S,3R,4S,6R)-3,4-epoxy-3,7,7-trimethylbicyclo[4.1.0]heptane 
• 54831-63-9 (-)-cis-caran-trans-4-amine 
• 555-31-7 aluminum isopropoxide 
• 67-63-0 isopropyl alcohol 
• 88390-12-9 (-)-cis-car-2-en-4-ol 

Downstream Products

• 4176-02-7 (-)-cis-Caran-3-on-semicarbazon 
• 5208-49-1 cis-4-carene 
• 6909-21-3 (-)-cis-Caran-trans-(5)-ol 
• 4017-88-3 4-isocaranol 
• 499-70-7 methyl-2 isopropyl-5 cyclohexanone 
• 4176-01-6 cis-carane-4-one 
• 499-70-7 methyl-2 isopropyl-5 cyclohexanone 
• 95242-32-3 2,5,5-trimethylcycloheptanone 
• 4176-01-6 (-)-isocaranone 
• 5208-43-5 toluene-4-sulfonic acid-((1S,3R,4S)-caran-4-yl ester) 
• 4175-97-7 4-nitro-benzoic acid-((1S,3R,4S)-caran-4-yl ester) 
• 6617-28-3 phthalic acid mono-((1S,3R,4S)-caran-4-yl ester) 

Relevant articles and documents

Synthesis of Some 4-Cyanocaranes

Four optically active 4-cyanocaranes diastereoisomers have been synthesized starting from (+)-car-3-ene and their structures supported by chemical evidences and X-ray analysis.

Novel Method for Hydroboration of Olefins Using Electrolysis

A first example of electrochemical hydroboration of olefins was found.Anodic oxidation of sodium borohydride in the presence of olefins in diglyme followed by conventional oxidation gave the corresponding alcohols regio- and stereoselectively in good yields.