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5,7-Octadien-2-ol, 2,6-dimethyl-, (5Z)-, also known as linalool, is a naturally occurring organic compound with the molecular formula C10H18O. It is a colorless to pale yellow liquid with a strong, sweet, floral scent. Linalool is a terpene alcohol, which is a class of organic compounds derived from isoprene units. It is widely found in various plants, such as lavender, coriander, and citrus fruits, and is also produced synthetically for use in the fragrance and flavor industries. Linalool has various applications, including its use as a fragrance component in perfumes, soaps, and cosmetics, as well as a flavoring agent in food and beverages. Additionally, it has been studied for its potential therapeutic properties, such as antimicrobial, anti-inflammatory, and analgesic effects.

7643-59-6

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7643-59-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7643-59-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,4 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7643-59:
(6*7)+(5*6)+(4*4)+(3*3)+(2*5)+(1*9)=116
116 % 10 = 6
So 7643-59-6 is a valid CAS Registry Number.

7643-59-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dimethylocta-5,7-dien-2-ol

1.2 Other means of identification

Product number -
Other names cis-Ocimenol

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:7643-59-6 SDS

7643-59-6Downstream Products

7643-59-6Relevant academic research and scientific papers

A PRACTICAL SYNTHESIS OF MYRCENOL BY PALLADIUM COMPLEX-CATALYZED ELIMINATION REACTION

Kumobayashi, Hidenori,Mitsuhashi, Shigeru,Akutagawa, Susumu,Ohtsuka, Sei

, p. 157 - 160 (2007/10/02)

A Palladium complex-catalyzed elimination reaction of allyl amines was studied to establish a practical process for production of myrcenol.The catalytic elimination occurred smoothly with the cationic Pd(II) complexes.Among a variety phosphorous ligands, the tetramethylene and the pentamethylene diphosphine ligands proved to be the best ligand with respects to the catalytic activity and selectivity.

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