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Pinocarveol, also known as [1S-(1-α-5-alpha)]6,6-dimethyl-2-methylenebicyclo[3.1.1]heptan-3-ol, is a naturally occurring monoterpene alcohol found in various plants, particularly in the essential oils of conifers such as pine and spruce. It is a colorless liquid with a strong, characteristic odor and is known for its insecticidal properties. Pinocarveol is used in the synthesis of various pharmaceuticals and agrochemicals, and it also has potential applications in the fragrance and flavor industries due to its unique scent. The chemical structure of pinocarveol consists of a bicyclic ring system with a hydroxyl group and a double bond, making it a versatile compound with a wide range of potential uses.

4955-29-7

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4955-29-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4955-29-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,5 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4955-29:
(6*4)+(5*9)+(4*5)+(3*5)+(2*2)+(1*9)=117
117 % 10 = 7
So 4955-29-7 is a valid CAS Registry Number.

4955-29-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-pinocarvyl acetate

1.2 Other means of identification

Product number -
Other names (1S:3R)-3-Acetoxy-pinen-(2(10))

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4955-29-7 SDS

4955-29-7Relevant academic research and scientific papers

Reactions of epoxides prepared from some monoterpenes with acetic anhydride on aluminosilicate catalysts

Tatarova,Korchagina,Volcho,Salakhutdinov,Barkhash

, p. 1076 - 1082 (2007/10/03)

Reactions of epoxides prepared from α-, β-pinenes and camphene with acetic anhydride on aluminosilicate catalysts (clay K-10, zeolite β) were investigated affording various products of skeleton rearrangements: mono- and diacetates with five- and six-membered rings, and also with norbornane and pinane cores.

PALLADIUM-CATALYZED ALLYLIC OXIDATION OF OLEFINS BY t-BUTYL HYDROPEROXIDE AND TELLURIUM(IV) OXIDE

Uemura, Sakae,Fukuzawa, Shin-ichi,Toshimitsu, Akio,Okano, Masaya

, p. 87 - 90 (2007/10/02)

Treatment of several cyclic olefins, β-pinene, allylbenzene and estragole with palladium(II) salt in acetic acid in the presence of t-butyl hydroperoxide and tellurium(IV) oxide afforded mainly the corresponding allylic acetates.The reaction proceeded catalytically with palladium(II) salt, t-BuOOH working as a reoxidazing agent.

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