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5,9,13-Pentadecatrien-2-one, 6,10,14-trimethyl-, (Z,E)- is a complex organic compound with the molecular formula C18H32O. It is a conjugated diene ketone, characterized by the presence of three double bonds (two in the Z configuration and one in the E configuration) and three methyl groups at the 6th, 10th, and 14th carbon atoms. 5,9,13-Pentadecatrien-2-one, 6,10,14-trimethyl-, (Z,E)- is a member of the alkenones family, which are long-chain unsaturated ketones commonly found in the lipids of haptophyte algae. The specific structure of 5,9,13-Pentadecatrien-2-one, 6,10,14-trimethyl-, (Z,E)-, with its alternating double bonds and methyl groups, contributes to its unique chemical properties and potential applications in various fields, such as biochemistry and organic synthesis.

1117-51-7

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1117-51-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1117-51-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,1 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1117-51:
(6*1)+(5*1)+(4*1)+(3*7)+(2*5)+(1*1)=47
47 % 10 = 7
So 1117-51-7 is a valid CAS Registry Number.

1117-51-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (5Z,9E)-6,10,14-trimethylpentadeca-5,9,13-trien-2-one

1.2 Other means of identification

Product number -
Other names .(5Z,9E)-6,10,14-trimethyl-pentadeca-5,9,13-trien-2-one

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:1117-51-7 SDS

1117-51-7Relevant academic research and scientific papers

PROCESS FOR THE PREPARATION OF (E, E)-FARNESYL ACETONE

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Page/Page column 4-5, (2009/04/25)

A process for the preparation of E-farnesyl acetone characterized by reaction of nerolidol with isopropenylmethyl ether in the presence of an acidic catalyst at elevated temperature and isolation by fractionated distillation.

-SIGMATROPIC REARRANGEMENTS OF THE ACETOACETATES OF ALLYL ALCOHOLS (CARROLL REACTION) AND ALLYLPHENYL ETHERS (CLAISEN REACTION) ON THE SURFACE OF ADSORBENTS

Pogrebnoi, S. I.,Kal'yan, Yu. B.,Krimer, M. Z.,Smit, V. A.

, p. 733 - 739 (2007/10/02)

A method has been developed for effecting rearrangements of allylacetoacetates to γ,δ-unsaturated ketones (Carroll rearrangement) and allylaryl ethers to the corresponding allylphenols (Claisen rearrangement) under conditions of adsorption on aluminum oxide and silica gel.The method provides a sharp reduction of the temperature of these reactions and improvement of their efficiency.

Allylic Carbonates. Efficient Allylating Agents of Carbonucleophiles in Palladium-Catalyzed Reactions under Neutral Conditions

Tsuji, Jiro,Shimizu, Isao,Minami, Ichiro,Ohashi, Yukihiro,Sugiura, Teruo,Takahashi, Kazuhiko

, p. 1523 - 1529 (2007/10/02)

Allylation of β-keto esters or malonates was carried out in good yields under neutral conditions by using allylic carbonates in the presence of palladium-phospine catalyst.Although simple ketones, esters, nitriles, and sulfones hardly react with allylic carbonates, α-alkenyl or α-aryl ketones, esters, nitriles, and sulfones were also allylated by using palladium-bis(diphenylphosphino)ethane catalyst under neutral conditions.

ORGANIC SYNTHESES WITH SULFONES (PART XXVIII) ;SYNTHESIS OF TERPENOID COMPOUNDS BY WAY OF MICHAEL ADDITION REACTIONS TO CONJUGATED DIENYL SULFONES.

Julia, M.,Lave, D.,Mulhauser, M.,Ramirez-Munoz, M.,Uguen, D.

, p. 1783 - 1786 (2007/10/02)

Michael additions of ethanol and ketones to allyl-dienyl sulfones yielded di-allylic sulfones which were transformed into isoprenoid compounds by either Ramberg-Baecklund reaction or thermolysis.

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