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3(15),7(14),10-Bisabolatriene is a naturally occurring sesquiterpene compound, characterized by its unique structure and properties. It is derived from the essential oils of various plants, particularly those belonging to the Asteraceae family, such as Matricaria chamomilla (German chamomile) and Anthemis nobilis (Roman chamomile). 3(15),7(14),10-Bisabolatriene exhibits a wide range of biological activities, including anti-inflammatory, antifungal, and antioxidant properties. Its chemical structure consists of a tricyclic sesquiterpene with a carbon skeleton of 15 carbon atoms, featuring two double bonds at positions 3 and 7, and a cyclopropane ring at positions 10 and 14. Due to its diverse therapeutic potential, 3(15),7(14),10-Bisabolatriene has been extensively studied for its applications in pharmaceuticals, cosmetics, and aromatherapy.

6009-90-1

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6009-90-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6009-90-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,0 and 9 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6009-90:
(6*6)+(5*0)+(4*0)+(3*9)+(2*9)+(1*0)=81
81 % 10 = 1
So 6009-90-1 is a valid CAS Registry Number.

6009-90-1SDS

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 iso-bisabolene

1.2 Other means of identification

Product number -
Other names 1-Methylene-4-(5-methyl-1-methylene-hex-4-enyl)-cyclohexane

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:6009-90-1 SDS

6009-90-1Downstream Products

6009-90-1Relevant academic research and scientific papers

CHEMISTRY OF THE ORGANOSILICON COMPOUNDS-165 2-TRIMETHYLSILYL-METHYL-1, 3-BUTADIENE-A VERSATILE BUILDING BLOCK FOR TERPENE SYNTHESIS

Sakurai, Hideki,Hosomi, Akira,Saito, Masaki,Sasaki, Koshi,Iguchi, Hirokazu,et al.

, p. 883 - 894 (2007/10/02)

Two types of synthetically useful reactions of 2-trimethylsilylmethyl-1,3-butadiene (7) are discussed.Reactions of 7 with acid chlorides, aldehydes, ketones and acetals activated by a Lewis acid give isoprenylated compounds, while 7 undergoes the Diels-Alder reaction whit dienophiles.High regiospecificity of the reaction qualifies 7 for a versatile building block of terpene synthesis.

HIGHLY REGIOSELECTIVE DIELS-ALDER REACTIONS OF 2-TRIMETHYLSILYLMETHYL-1,3-BUTADIENE CATALYZED BY A LEWIS ACID AND APPLICATIONS TO SYNTHESES OF TERPENES

Hosomi, Akira,Iguchi, Hirokazu,Sasaki, Jun-ichi,Sakurai, Hideki

, p. 551 - 554 (2007/10/02)

2-Trimethylsilylmethyl-1,3-butadiene undergoes highly regioselective Diels-Alder reactions with dienophiles such as acrolein and methyl vinyl ketone catalyzed by aluminium chloride in which the "para" isomers are obtained almost exclusively.The adducts are converted readily to a variety of naturally occurring mono and sesquiterpenes.

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