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3,6-Octadien-1-ol, 3,7-dimethyl- is a naturally occurring organic compound with the chemical formula C10H18O. It is a colorless liquid with a strong, sweet, and floral odor. 3,6-Octadien-1-ol, 3,7-dimethyl- is commonly found in various essential oils, such as lavender, rose, and jasmine, and is used in the fragrance industry as a fixative and scent enhancer. It is also known as linalool, which is a key component in many perfumes and cosmetics due to its pleasant aroma. Linalool is derived from various plant sources and can be synthesized chemically as well. It is considered safe for use in fragrances and has been extensively studied for its potential therapeutic properties, including anti-inflammatory and antimicrobial effects.

7779-06-8

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7779-06-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7779-06-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,7 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7779-06:
(6*7)+(5*7)+(4*7)+(3*9)+(2*0)+(1*6)=138
138 % 10 = 8
So 7779-06-8 is a valid CAS Registry Number.

7779-06-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,7-dimethylocta-3,6-dien-1-ol

1.2 Other means of identification

Product number -
Other names 3,6-Octadien-1-ol,3,7-dimethyl

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:7779-06-8 SDS

7779-06-8Downstream Products

7779-06-8Relevant academic research and scientific papers

ON THE ROLE OF THE PHOSPHATE RESIDUES IN GERANYL PYROPHOSPHATE BIOSYNTHESIS

Jacob, L.,Julia, M.,Pfeiffer, B.,Rolando, C.

, p. 4327 - 4330 (2007/10/02)

Phosphoric esters bearing a sulfonium group in the γ position are converted under basic conditions into allylic phosphates.

BIOMIMETIC ENTRY TO ACYCLIC TERPENE SYNTHESIS. A NOVEL REARRANGEMENT OF ALLYL ETHER CATALYZED BY ORGANOALUMINUM REAGENTS

Yamamura, Yoshihiro,Umeyama, Kensuke,Maruoka, Keiji,Yamamoto, Hisashi

, p. 1933 - 1936 (2007/10/02)

The intramolecular prenyltransfer reaction is accomplished by the rearrangement of allyl ethers with (2,6-di-tert-butyl-4-methylphenoxy)methylaluminum trifluoromethanesulfonate.The present method provides a simple and highly efficient synthesis of lavandulol.

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