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3,5,9-Undecatrien-2-one, 6,10-dimethyl-, (Z,Z)- is a chemical compound with the molecular formula C13H20O. It is an organic compound characterized by the presence of three double bonds in its carbon chain, specifically at the 3rd, 5th, and 9th positions. The compound also features two methyl groups attached to the 6th and 10th carbon atoms, respectively. The (Z,Z) notation indicates that the double bonds have the Z configuration, meaning that the substituents on each double bond are on the same side when viewed from the priority end of the molecule. 3,5,9-Undecatrien-2-one, 6,10-dimethyl-, (Z,Z)- is known for its unique structure and potential applications in various chemical and industrial processes.

3796-54-1

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3796-54-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3796-54-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,9 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3796-54:
(6*3)+(5*7)+(4*9)+(3*6)+(2*5)+(1*4)=121
121 % 10 = 1
So 3796-54-1 is a valid CAS Registry Number.

3796-54-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (3Z,5Z)-6,10-dimethylundeca-3,5,9-trien-2-one

1.2 Other means of identification

Product number -
Other names 3Z,5Z-Pseudoionone

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:3796-54-1 SDS

3796-54-1Relevant academic research and scientific papers

(6R,10R)-6,10,14-TRIMETYLPENTADECAN-2-ONE PREPARED FROM 6,10-DIMETYLUNDECA-3,5,9-TRIEN-2-ONE

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Page/Page column 37; 38, (2014/07/08)

The present invention relates to a process of manufacturing (6R,10R) -6,10,14-trimethylpentadecan-2-one in a multistep synthesis from 6,10- dimethylundeca-3,5,9-trien-2-one. The process is very advantageous in that it forms in an efficient way the desired chiral product from a mixture of stereoisomers of the starting product.

Photochemical transformations of terpenoids in the presence of cyclodextrins

Luzina,Tatarova,Korchagina,Salakhutdinov,Barkhash

, p. 183 - 193 (2007/10/03)

The effect of complexation of terpene compounds with cyclodextrins on photolysis depends on the type of cyclodextrin and on the structure of the initial substrates. In some cases, only a change in the reaction rate is observed; in other cases, the complexation results in allylic rearrangements, hydride and acyl shifts, and cyclization with the formation of four-, five-, and six-membered cycles, whereas only cis-trans isomerization reactions are observed in the absence of complexation.

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