5163-67-7

Basic information

• Product Name: (E)-oct-3-enoic acid
• Synonyms: (E)-oct-3-enoic acid;(E)-3-Octenoic acid;Einecs 225-941-6
• CAS NO: 5163-67-7
• Molecular Formula: C₈H₁₄O₂
• Molecular Weight: 142.19556
• EINECS: 225-941-6
• Mol File: 5163-67-7.mol
• Article Data: 15

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (E)-oct-3-enoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-oct-3-enoic acid(5163-67-7)
• EPA Substance Registry System: (E)-oct-3-enoic acid(5163-67-7)

Safety Data

• Hazardous Substances Data: 5163-67-7(Hazardous Substances Data)

Usage

General Description

(E)-Oct-3-enoic acid, also known as (E)-3-Octenoic acid, is a naturally occurring organic compound belonging to the family of unsaturated fatty acids. It is a colorless liquid with a characteristic unpleasant odor and is found in various plant and animal sources. The chemical formula of (E)-Oct-3-enoic acid is C8H14O2 and it is classified as a carboxylic acid due to the presence of the carboxyl functional group. (E)-Oct-3-enoic acid is used as a flavoring agent in food products and as a chemical intermediate in the production of various types of esters and other compounds. Additionally, (E)-Oct-3-enoic acid has been found to have antibacterial properties and is under research for potential medical and pharmaceutical applications.

InChI:InChI=1/C8H14O2/c1-2-3-4-5-6-7-8(9)10/h5-6H,2-4,7H2,1H3,(H,9,10)/b6-5+

Upstream product

• 57074-96-1 oct-3-ynoic acid 
• 32359-01-6 hexenylmagnesium bromide 
• 14916-80-4 oct-3-yn-1-ol 
• 18185-81-4 cis-3-octen-1-ol 
• 78693-34-2 (Z)-deca-1,5-dien-3-ol 
• 4938-52-7 1-hepten-3-ol 
• 201230-82-2 carbon monoxide 
• 18185-81-4 (E)-oct-3-en-1-ol 
• 110-62-3 pentanal 
• 51114-94-4 (2-carboxyethyl)triphenylphosphonium bromide 
• 141-82-2 malonic acid 
• 66-25-1 hexanal 

Downstream Products

• 35234-16-3 (E)-methyl oct-3-enoate 
• 26553-47-9 Ethyl (E)-3-octenoate 
• 1470-50-4 oct-2-enoic acid 
• 126442-53-3 (S)-3-hydroxyoctanoic acid benzyl ester 
• 33796-86-0 (S)-3-hydroxyoctanoic acid 
• 44987-72-6 (R)-3-hydroxy-octanoic acid 
• 1016225-19-6 (S)-3-hydroxyoctanoic acid phenyl amide 
• 1262032-25-6 (E)-N-tosyl-3-octenamide 
• 133910-57-3 (E)-3-octenoic acid benzylamide 
• 125763-06-6 3-phenyl-trans-4-butyl-5-<(methoxycarbonyl)methyl>-1,3-oxazolidin-2-one 
• 53963-09-0 (7Z,11E)-hexadeca-7,11-dien-1-ol 
• 23192-82-7 (E)-tetradec-9-en-1-yl acetate 
• 53155-10-5 (E)-1-oct-3-enyl bromide 
• 53042-79-8 1-acetoxyhexadeca-7Z,11E-diene 

Relevant articles and documents

On the stereoselection of iodolactonizations of 3-silyloxyalk-5-enoic acids

Iodolactonizations of 3-triisopropylsilyloxyalk-5-enoic acids (10b and 12) proceed by way of common transition-state geometry 23, in which the silyloxy group is positioned axially, presumably due to hydrogen bonding with the carboxylic acid group.

Enantioselective Alkylamination of Unactivated Alkenes under Copper Catalysis

An enantioselective addition reaction of various alkyl groups to unactivated internal alkenes under Cu catalysis has been developed. The reaction uses amide-linked aminoquinoline as the directing group, 4-alkyl Hantzsch esters as the donor of alkyl radicals, and rarely used biaryl diphosphine oxide as a chiral ligand. β-lactams featuring two contiguous stereocenters at Cβ and the β substituent can be obtained in good yield with excellent enantioselectivity. Mechanistic studies indicate that a nucleophilic addition of the alkyl radical to CuII-coordinated alkene is the enantio-determining step.

PROCESS FOR THE PREPARATION OF UNSATURATED CARBOXYLIC ACIDS BY CARBONYLATION OF ALLYL ALCOHOLS AND THEIR ACYLATION PRODUCTS

The present invention relates to a process for carbonylating allyl alcohols at low temperature, low pressure and/or low catalyst loading. In an alternative embodiment, an acylation product of the allyl alcohol is used for the carbonylation. The present invention likewise relates to the preparation of conversion products of these carbonylation products and specifically of (?)-ambrox.