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17910-09-7

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17910-09-7 Usage

General Description

Curzerene is a naturally occurring chemical compound primarily found in several types of plants, notably the Curcuma genus, which includes turmeric. It's a sesquiterpene, a class of organic compounds often used in aromatherapy and alternative medicine for their potential therapeutic effects. Several studies suggest that curzerene may have anti-inflammatory, antimicrobial, and anticancer properties. However, more research is needed to fully understand its benefits and potential uses in medicine or other industries.

Check Digit Verification of cas no

The CAS Registry Mumber 17910-09-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,1 and 0 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17910-09:
(7*1)+(6*7)+(5*9)+(4*1)+(3*0)+(2*0)+(1*9)=107
107 % 10 = 7
So 17910-09-7 is a valid CAS Registry Number.

17910-09-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name isofuranogermacrene

1.2 Other means of identification

Product number -
Other names Curzerene

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:17910-09-7 SDS

17910-09-7Relevant articles and documents

TOTAL SYNTHESIS OF VARIOUS ELEMANOLIDES

Friedrich, Dirk,Bohlmann, Ferdinand

, p. 1369 - 1392 (2007/10/02)

Starting with a suitable substituted divinyl cyclohexanone, eleven naturally occurring 12.8-elemanolides bearing exo-methylene or methyl groups at C-11 and differing in substitution as well as in relative configuration, have been synthesized in racemic form.An approach to elemanolides with additional oxygen functionalities is principally possible by modification of the basic concept.Methods for the oxidative generation of terpenoid exo-methylene lactone and furan units are exemplified by synthesis of menthofuran and the p-menthenolides from isopulegols.

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