What is the 2-pinen-7-one?

2-pinen-7-one is , while it's Molecular Formula is C 10 H 14 O.

What is the CAS number for 2-pinen-7-one?

The CAS number of 2-pinen-7-one is 473-06-3.

What is 2-pinen-7-one (473-06-3) used for?

2-Pinene-7-one, also known as 2-carenone, is a bicyclic monoterpene ketone found in various essential oils, particularly in the oils of pine, fir, and other coniferous plants. It is a colorless to pale yellow liquid with a strong, pungent odor. This organic compound has a molecular formula of C10H16O and a molecular weight of 152.23 g/mol. 2-Pinene-7-one is known for its insecticidal properties and is used in the synthesis of various fragrances, flavorings, and pharmaceuticals. It is also recognized for its potential anti-inflammatory and antimicrobial activities, making it a subject of interest in the field of natural product chemistry and potential applications in medicine and agriculture.

What is the 2-pinen-7-one?

2-pinen-7-one is , while it's Molecular Formula is C 10 H 14 O.

What is the CAS number for 2-pinen-7-one?

The CAS number of 2-pinen-7-one is 473-06-3.

What is 2-pinen-7-one (473-06-3) used for?

2-Pinene-7-one, also known as 2-carenone, is a bicyclic monoterpene ketone found in various essential oils, particularly in the oils of pine, fir, and other coniferous plants. It is a colorless to pale yellow liquid with a strong, pungent odor. This organic compound has a molecular formula of C10H16O and a molecular weight of 152.23 g/mol. 2-Pinene-7-one is known for its insecticidal properties and is used in the synthesis of various fragrances, flavorings, and pharmaceuticals. It is also recognized for its potential anti-inflammatory and antimicrobial activities, making it a subject of interest in the field of natural product chemistry and potential applications in medicine and agriculture.

473-06-3

Product NameC09843473-06-3
Molecular FormulaC₁₀H₁₄O
Molecular Weight150.221
Purity99%

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Product Details

Quick Details

CasNo： 473-06-3
Molecular Formula： C₁₀H₁₄O
Purity： 99%

Chinese Manufacturer supply C09843473-06-3 473-06-3 in stock with high standard

Molecular Formula:C₁₀H₁₄O
Molecular Weight:150.221
Vapor Pressure:0.204mmHg at 25°C
Boiling Point:209.3°C at 760 mmHg
Flash Point:76.3°C
Density:0.992g/cm³

473-06-3 Relevant articles

Synthesis of Terpenes Containing the Bicycloheptane Ring System by the Intramolecular Cycloaddition Reaction of Vinylketenes with Alkenes. Preparation of Chrysanthenone, β-Pinene, β-cis-Bergamotene, β-trans-Bergamotene, β-Copaene, and β-Ylangene and Lemnalol

Kulkarni, Yashwant S.,Niwa, Maho,Ron, Eyal,Snider, Barry B.

, p. 1568 - 1576 (2007/10/02)

Treatment of geranoyl chloride (20) with...

Intramolecular Cycloadditions of Ketenes. 2. Synthesis of Crysanthenone, β-Pinene, β-cis-Bergamotene, and β-trans-Bergamotene

Kulkarni, Yashwant S.,Snider, Barry B.

, p. 2809 - 2810 (2007/10/02)

Vinylketenes prepared from geranoyl and ...

473-06-3 Process route

: 4698-08-2
(E)-geranic acid

: 473-06-3,38301-80-3,58437-73-3,97169-74-9
chrysanthenone

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: oxalyl chloride / benzene / a) 25 deg C, 2 h, b) 45 deg C, 30 min 2: 2 percent / Et₃N / toluene / 3 h / Heating With oxalyl dichloride; triethylamine; In toluene; benzene;
Multi-step reaction with 3 steps 1: oxalyl chloride / benzene / a) 25 deg C, 2 h, b) 45 deg C, 30 min 2: 43 percent / Et₃N / toluene / 3 h / Heating 3: 95 percent / H₂ / 5percent Pd/CaCO₃ / hexane / 0.17 h / 25 °C With oxalyl dichloride; hydrogen; triethylamine; Lindlar's catalyst; In hexane; toluene; benzene;
Multi-step reaction with 3 steps 1: oxalyl chloride / benzene / 2 h / 25 °C 2: 43 percent / NEt₃ / toluene / 1 h / Heating 3: 100 percent / H₂ / palladium on calcium carbonate With oxalyl dichloride; hydrogen; triethylamine; palladium on activated charcoal; In toluene; benzene;
Multi-step reaction with 3 steps 1: oxalyl chloride / benzene / a) 25 deg C, 2 h, b) 45 deg C, 30 min 2: 43 percent / Et₃N / toluene / 3 h / Heating 3: 95 percent / H₂ / 5percent Pd/CaCO₃ / hexane / 0.17 h / 25 °C With oxalyl dichloride; hydrogen; triethylamine; Lindlar's catalyst; In hexane; toluene; benzene;