5445-29-4

Usage

Uses

Used in Flavor and Fragrance Industry:
Ethyl 2-bromooctanoate is used as a flavoring agent and fragrance ingredient for its distinctive fruity scent, enhancing the sensory experience of various consumer products.
Used in Pharmaceutical Industry:
Ethyl 2-bromooctanoate is used as an intermediate in the production of pharmaceuticals, contributing to the synthesis of various medicinal compounds.
Used in Pesticide Industry:
Ethyl 2-bromooctanoate is utilized as an intermediate in the manufacturing process of pesticides, playing a role in the development of agricultural chemicals aimed at controlling pests.

InChI:InChI=1/C10H19BrO2/c1-3-5-6-7-8-9(11)10(12)13-4-2/h9H,3-8H2,1-2H3/t9-/m1/s1

Upstream product

• 64-17-5 ethanol 
• 124-07-2 Octanoic acid 
• 2623-82-7 2-bromooctanoic acid 
• 7664-93-9 sulfuric acid 
• 106265-08-1 2-bromooctanoyl bromide 
• 83818-62-6 1-chloro-1-(phenylthio)-1-octene 
• 59176-56-6 1-Methylthio-1-(trimethylsilyl)-1-octen 

Downstream Products

• 40843-12-7 4-(4-Chlorphenoxy)-α-phenoxy-caprylsaeure 
• 51337-96-3 2-[4-(4-Chloro-phenoxy)-phenoxy]-octanoic acid ethyl ester 
• 63538-11-4 2-{4-[4-(1-Ethoxycarbonyl-heptyloxy)-phenylsulfanyl]-phenoxy}-octanoic acid ethyl ester 
• 63538-38-5 2-{4-[4-(1-Ethoxycarbonyl-heptyloxy)-benzenesulfonyl]-phenoxy}-octanoic acid ethyl ester 
• 63538-37-4 2-{4-[4-(1-Ethoxycarbonyl-heptyloxy)-benzenesulfinyl]-phenoxy}-octanoic acid ethyl ester 
• 63538-26-1 2-{2-Chloro-4-[3-chloro-4-(1-ethoxycarbonyl-heptyloxy)-phenoxy]-phenoxy}-octanoic acid ethyl ester 
• 63538-29-4 2-{2-Bromo-4-[3-bromo-4-(1-ethoxycarbonyl-heptyloxy)-phenoxy]-phenoxy}-octanoic acid ethyl ester 
• 63538-28-3 2-{2,6-Dichloro-4-[3,5-dichloro-4-(1-ethoxycarbonyl-heptyloxy)-phenoxy]-phenoxy}-octanoic acid ethyl ester 
• 7597-88-8 2-(1,1,3-trioxo-1,3-dihydro-1λ⁶-benzo[d]isothiazol-2-yl)-octanoic acid ethyl ester 
• 40226-04-8 ethyl 2-(diethoxyphosphoryl)octanoate 
• 2351-90-8 Ethyl oct-2-enoate 
• 7740-65-0 Ethyl 2-fluorooctanoate 
• 128849-99-0 2-(Acetoxy-phenyl-methyl)-octanoic acid ethyl ester 
• 188699-85-6 2-[2-({3-[(E)-2-(7-Chloro-quinolin-2-yl)-vinyl]-phenylamino}-methyl)-phenoxy]-octanoic acid ethyl ester 

Relevant academic research and scientific papers

Highly selective synthesis of α-bromoesters using molecular bromine catalyzed by phosphorus

A series of α-bromoesters have been synthesized by applying Hell-Volhard-Zelinsky reaction catalyzed by phosphorus instead of usual phosphorus tribromide. An excellent regioselectivity to good yields are achieved at comparatively mild reaction conditions of an operational simplicity.

Cosmetic compositions

A composition for application to human skin to enhance elasticity contains as active ingredient a sulphur-containing compound of the general formula: in which M is hydrogen or a water-solubilising cation, X is S, and Y is alkyl or alkenyl of up to 4 carbon atoms, or else -XY is -SH.

SOLVOLYSIS OF 1-CHLORO-1-ALKENYL PHENYL SULFIDES. SYNTHESIS OF α-BROMO PHENYL THIOCARBOXYLIC ESTERS, α-BROMO ALKYL CARBOXYLIC ESTERS AND α-PHENYLTHIO METHYL CARBOXYLIC ESTERS

1-Chloro-1-alkenyl phenyl sulfides treated with bromine followed by hydrolysis or methanolysis give α-bromo phenyl thiocarboxylic esters and α-phenylthio methyl carboxylic esters.Direct oxidative solvolysis with bromine and alcohol give α-bromo alkyl carboxylic esters.

Unnatural nucleosides and nucleotides. III. Preparation of 2-14C and 4-14C labelled 5-alkyluracils and 5-alkyl-2'-deoxyuridines

2-14C Labelled 5-alkyluracils were prepared by condensation of the diethylacetals of α-formyl-carbonic acid esters with 14C-thiourea. Compounds labelled at 4-C were synthesized by condensation of the labelled carboxylic acid derivatives with thiourea. β-Anomers of 5-alkyl-2'-deoxyuridines were obtained in a fairly good radiochemical yield. Alkyl substituents ranged from methyl to tetradecyl, isopropyl and tert-butyl.