473-61-0

Basic information

• Product Name: cis-pinocampheol
• CAS NO: 473-61-0
• Molecular Formula: C₁₀H₁₈O
• Mol File: 473-61-0.mol
• Article Data: 21

Chemical Properties

• CAS DataBase Reference: cis-pinocampheol(CAS DataBase Reference)
• NIST Chemistry Reference: cis-pinocampheol(473-61-0)
• EPA Substance Registry System: cis-pinocampheol(473-61-0)

Safety Data

• Hazardous Substances Data: 473-61-0(Hazardous Substances Data)

Usage

General Description

Cis-pinocampheol is a naturally occurring chemical compound found in the oils of certain conifer trees, particularly pine and fir trees. It is classified as a bicyclic monoterpene alcohol and is known for its characteristic pine-like aroma. Cis-pinocampheol is commonly used in the fragrance and flavoring industries to impart a fresh, woody, and resinous scent to a wide range of products, including perfumes, soaps, and household cleaners. It also has potential medicinal properties, with research suggesting it may have antioxidant and anti-inflammatory effects. Additionally, cis-pinocampheol has been identified as a significant component of several essential oils used in traditional medicine for its possible therapeutic benefits.

Upstream product

• 19894-98-5 6,6-dimethyl-2-methylene-bicyclo[3.1.1]heptan-3-ol 
• 1686-14-2 (1R,2R,4S,6R)-2,7,7-trimethyl-3-oxatricyclo[4.1.1.0.^2,4]octane 
• 110-82-7 cyclohexane 
• 1058019-16-1 C₁₃H₂₀O 
• 21947-87-5 L-diisopinocampheylborane 
• 18358-53-7 pinocamphone 
• 873-66-5 1-propenylbenzene 
• 103-30-0 (E)-1,2-diphenyl-ethene 
• 768-49-0 (2-methyl-1-propenyl)-benzene 
• 767-99-7 (Z)-2-phenylbut-2-ene 
• 768-00-3 (E)-2-phenyl-2-butene 
• 4165-78-0 (Z)-(1-ethylpropenyl)benzene 
• 4165-86-0 (E)-(1-ethylpropenyl)benzene 
• 80-56-8 Pinene 

Downstream Products

• 14575-93-0 isopinocamphone 
• 14575-99-6 phthalic acid mono-((1S:2S:3S)-pinanyl-⁽³⁾-ester) 
• 473-62-1 trans-pinocamphone 
• 102992-45-0 (1RS:2SR:3SR)-3-phenylcarbamoyloxy-pinane 
• 5362-50-5 4-methyl-3-penten-1-al 
• 36237-64-6 dihydrocarveol 
• 39166-57-9 (+)-isopinocampheyl acetate 
• 257950-76-8 (1RS,2RS,1'R,2'S,3'R)-trans-2-pinanylthiocyclohexanol 
• 257950-78-0 (-)-(1R,2R,S_S,1'R,2'S,3'R)-trans-2-pinanylsulfinylcyclohexanol 
• 155257-69-5 (1R,2R,6S,8R)-2,9,9-Trimethyl-3-[(E)-(3-phenyl-acryloyl)]-5-oxa-3-aza-tricyclo[6.1.1.0^2,6]decan-4-one 

Relevant articles and documents

Preparation of crystalline (diisopinocampheyl)borane

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Synthesis and ultraviolet absorption characteristics of 4-arylidene isopinocamphones from α-pinene

A new series of 4-arylidene isopinocamphones were synthesized from α-pinene which is a natural chemical from pine tree and their ultraviolet absorption characteristics were investigated. (+)Isopinocamphone was obtained from α-pinene by hydroboration-oxidation and then it was reacted with benzaldehyde, p-methylbenzaldehyde, p -methoxybenzaldehyde, p-chlorobenzaldehyde, furfural and p -nitrobenzaldehyde in the presence of alkali catalysts to get 4-arylidene isopinocamphones including 2-benzylidene-4,6,6-trimethylbicyclo[3.1.1]heptan-3-one (1), 2,6,6-trimethyl-4-(4-methyl benzyl)bicyclo[3.1.1]heptane-3-one (2), 2-(4-methoxybenzylidene)-4,6,6-trimethylbicyclo[3.1.1] heptan-3-one ( 3 ), 2-(4-chlorobenzylidene)-4,6,6-trimethylbicyclo[3.1.1]heptan-3-one (4 ), 2-(furan-2-methylene)-4,6,6-trimethylbicyclic [3.1.1] heptane-3-one (5) and 2,6,6-trimethyl-4-(4-nitrobenzylidene)bicyclo[3.1.1]heptan-3-one (6). he structures of 4-arylidene isopinocamphones were determined by FT-IR, 1H NMR, 13/C NMR and GC-MS technique. Their ultraviolet absorption characteristics and light stability was further examined. The results showed that compounds 1 , 2, 3 and 5 could be used as Btype UV absorbents, compounds 4 and 6 could be used as A-type UV absorbents and compounds 6 had both functions as UV-A and UVB types absorbents. The light stability sequence of these compounds was (2 ) > (1) ≈ (3) ≈ (4) ≈(6) > (5).

Synthesis of (+)-B-allyldiisopinocampheylborane and its reaction with aldehydes

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