13307-34-1

Basic information

• Product Name: alpha-methylbicyclo[2.2.1]hept-5-ene-2-methanol
• Synonyms: alpha-methylbicyclo[2.2.1]hept-5-ene-2-methanol;α-Methylbicyclo[2.2.1]hept-5-ene-2-methanol
• CAS NO: 13307-34-1
• Molecular Formula: C₉H₁₄O
• Molecular Weight: 138.20686
• EINECS: 236-333-5
• Mol File: 13307-34-1.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: alpha-methylbicyclo[2.2.1]hept-5-ene-2-methanol(CAS DataBase Reference)
• NIST Chemistry Reference: alpha-methylbicyclo[2.2.1]hept-5-ene-2-methanol(13307-34-1)
• EPA Substance Registry System: alpha-methylbicyclo[2.2.1]hept-5-ene-2-methanol(13307-34-1)

Safety Data

• Hazardous Substances Data: 13307-34-1(Hazardous Substances Data)

Usage

Bicyclic Structure

The compound has a bicyclic structure, specifically a bicyclo[2.2.1]heptane ring system.

Hydroxyl Functional Group

Contains a hydroxyl (-OH) functional group, making it an alcohol.

Essential Oils

Found in essential oils derived from coniferous trees such as pine, fir, and cypress.

Fragrance Industry

Used as a scent enhancer and fixative in perfumes.

Flavor Industry

Employed to enhance flavors.

Antimicrobial

Possesses antimicrobial properties.

Anti-inflammatory

Acts as an anti-inflammatory agent.

Bronchodilator

Used as a bronchodilator to help open up airways.

Pleasant, Woody Aroma

Known for its pleasant woody scent.

Perfumes

Often used in natural perfumes.

Air Fresheners

Included in air freshener formulations.

Household Cleaners

Used in some natural household cleaning products.

This list covers the key properties and uses of bornyl alcohol based on the information provided.

Upstream product

• 19926-90-0 (+/-)-endo-bicyclo[2.2.1]hept-5-ene-2-carbaldehyde 
• 74-88-4 methyl iodide 
• 917-64-6 methyl magnesium iodide 
• 5453-80-5 5-Norbornene-2-carboxaldehyde 

Downstream Products

• 5063-03-6 2-acetyl-5-norbornene 
• 13367-08-3 Bernsteinsaeure-methylester-<1-(bicyclo<2.2.1>hept-5-en-2-yl)-ethylester> 
• 13305-60-7 1-(Bicyclo<2.2.1>hept-5-en-2-yl)-ethan-1-ol-butyrat 
• 13305-29-8 2ξ-<1-Hydroxy-aethyl>-bicyclo<2.2.1>heptan 

Relevant articles and documents

Resolution of secondary alcohols by enzyme-catalyzed transesterification in alkyl carboxylates as the solvent

The Porcine Pancreatic Lipase (PPL)- and Mucor Esterase-catalyzed resolution of 1-phenylethanol 5 in four different alkyl carboxylate solvents, viz. methyl acetate, propionate and butyrate and ethyl acetate, was evaluated. The beneficial influence of the addition of molecular sieves 4A to the reaction mixture is demonstrated. A Mucor Esterase-catalyzed resolution of 5 on a 0.5 mol scale is described. The kinetic resolution of a large variety of secondary alcohols (5 - 22b) was investigated using both biocatalysts under the established optimal reaction conditions for substrate 5.