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3,7-dimethyl-1,7-octadien-3-ol, also known as linalool, is a naturally occurring organic compound that belongs to the terpene family. It is a colorless liquid with a floral scent and is widely found in various plants, such as lavender, coriander, and citrus fruits. Linalool is commonly used in the fragrance and flavor industry due to its pleasant odor, and it is also known for its potential therapeutic properties, such as anti-inflammatory, anti-microbial, and anti-depressant effects. The chemical structure of linalool consists of an eight-carbon chain with two methyl groups at the third and seventh positions, and a hydroxyl group at the third position, making it a valuable compound in both natural and synthetic applications.

598-07-2

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598-07-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 598-07-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 598-07:
(5*5)+(4*9)+(3*8)+(2*0)+(1*7)=92
92 % 10 = 2
So 598-07-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O/c1-5-10(4,11)8-6-7-9(2)3/h5,11H,1-2,6-8H2,3-4H3

598-07-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names 3,7-dimethyl-octa-1,7-dien-3-ol

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:598-07-2 SDS

598-07-2Relevant academic research and scientific papers

Intermediates for use in the preparation of vitamin E

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Example 8, (2008/06/13)

Novel intermediate compounds which can be used in the preparation of phytone and Vitamin E and a process for the preparation thereof. A process for the preparation of phytone and Vitamin E from these compounds is also claimed.

ELECTROPHILIC CYCLIZATION OF α-MONOTERPENOLS AS A MODEL FOR THE BIOSYNTHESIS OF TRI- AND TETRACYCLIC DITERPENES

Moiseenkov, A. M.,Veselovskii, V. V.,Dragan, V. A.,Ignatenko, A. V.,Strelenko, Yu. A.

, p. 1233 - 1237 (2007/10/02)

Low temperature electrophilic cyclization of α-geraniol, α-nerol, and α-linalool initiated by BF3*etherate leads to the formation of dimethylvinylcyclohexenes and bicyclooctyl fluoride, which have monoterpene skeletons.The α-monoterpenol starting materials may be regarded as close models to labdadienols, and their transformation as mimicking the biosynthesis of diterpenes in the pimarane and gibbane series according to Wenkert.

Alkylation du linalol sur les carbones C8 (et C6)

Cuvigny, Therese,Julia, Marc,Rolando, Christian

, p. 9 - 28 (2007/10/02)

Metallation of linalool α to the distal double bond with strong bases is described.The corresponding carbanions have been alkylated or oxidized to give mixtures of products resulting from attack at both carbon 8 (major product) and carbon 6 (minor product).

Palladium-catalyzed Reaction of Isoprene with Water in Presence of Carbon Dioxide and Base

Inoue, Yoshio,Sato, Michio,Satake, Masaki,Hashimoto, Harukichi

, p. 637 - 638 (2007/10/02)

Palladium(0)-catalyzed reaction of isoprene with water was enhanced by the presence of carbon dioxide and a base to give dimethyloctadienols.The same catalyst was found to dehydrate the dimethyloctadienols to afford the corresponding dimethyloctatrienes.The effect of acidity of water on the isoprene-water reaction was also studied.

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