94088-26-3

Usage

Uses

Used in Food Industry:
(2E,6Z)-dodeca-2,6-dienoic acid is used as a flavoring agent in the food industry. Its unique unsaturated structure contributes to the development of specific flavors and aromas in food products.
Used in Polymer and Resin Manufacturing:
(2E,6Z)-dodeca-2,6-dienoic acid is used as a raw material in the manufacturing of polymers and resins. Its unsaturated structure allows for the formation of strong and durable materials with various applications.
Used in Pharmaceutical Industry:
(2E,6Z)-dodeca-2,6-dienoic acid is used as an anti-inflammatory and antimicrobial agent in the pharmaceutical industry. Its potential biological and pharmacological properties make it a promising candidate for the development of new drugs and treatments.
Used in Industrial Chemical Production:
(2E,6Z)-dodeca-2,6-dienoic acid is used in the production of various industrial chemicals. Its versatile structure allows for its use in a wide range of chemical reactions and processes.

InChI:InChI=1/C12H20O2/c1-2-3-4-5-6-7-8-9-10-11-12(13)14/h6-7,10-11H,2-5,8-9H2,1H3,(H,13,14)/b7-6+,11-10+

Upstream product

• 141-82-2 malonic acid 
• 30390-50-2 4-decenal 

Relevant academic research and scientific papers

METHOD FOR THE DECARBOXYLATIVE HYDROFORMYLATION OF ALPHA, BETA- UNSATURATED CARBOXYLIC ACIDS

The present invention relates to a process for preparing aldehydes by reacting an α,β-unsaturated carboxylic acid or a salt thereof with carbon monoxide and hydrogen in the presence of a catalyst comprising at least one complex of a metal of transition group VIII of the Periodic Table of the Elements with at least one compound of the formula (I), where Pn is pnicogen; W is a divalent bridging group having from 1 to 8 bridge atoms between the flanking bonds; R1 is a functional group capable of forming at least one intermolecular, noncovalent bond with the —X(═O)OH group of the compound of the formula (I); R2, R3 are each in each case optionally substituted alkyl, cycloalkyl, heterocycloalkyl, aryl or hetaryl or together with the pnicogen atom and together with the groups Y2 and Y3 if present form an optionally fused and optionally substituted 5- to 8-membered heterocycle; a, b and c are each 0 or 1; and Y1,2,3 are each, independently of one another, O, S, NRa or SiRbRc, where Ra,b,c are each H or in each case optionally substituted alkyl, cycloalkyl, heterocycloalkyl, aryl or hetaryl; and the use of the above-described catalyst for the decarboxylative hydroformylation of α,β-unsaturated carboxylic acids.

A supramolecular catalyst for the decarboxylative hydroformylation of α,β-unsaturated carboxylic acids

(Chemical Equation Presented) Head 'em up, move 'em out, aldehyde! A catalytic transformation of α,β-unsaturated carboxylic acids into aldehydes through a hydroformylation-decarboxylation process has been developed (see scheme; Do = donor ligand, FG1 and FG2 = complementary functional groups). The reaction proceeds at mild conditions, tolerates many functional groups, and liberates CO2 as the only stoichiometric by-product.