615-96-3

Usage

Uses

Used in Chemical Synthesis:
Ethyl 2-bromohexanoate is used as an intermediate in the synthesis of various organic compounds for different applications. It serves as a building block for the preparation of other chemicals, which can be further utilized in various industries.
Used in Pharmaceutical Industry:
Ethyl 2-bromohexanoate is used as a synthetic intermediate for the production of pharmaceuticals. It can be used to synthesize various drug molecules, including antibiotics, anti-inflammatory agents, and other therapeutic compounds.
Used in Agrochemical Industry:
In the agrochemical industry, Ethyl 2-bromohexanoate is used as a precursor for the synthesis of various agrochemicals, such as pesticides and herbicides. It plays a crucial role in the development of new and effective crop protection agents.
Used in Flavor and Fragrance Industry:
Ethyl 2-bromohexanoate is used as a starting material for the synthesis of various flavor and fragrance compounds. It can be used to create unique scents and flavors for use in the food, beverage, and cosmetic industries.
Used in the Preparation of Ethyl 2,2-dibromohexanoate:
Ethyl 2-bromohexanoate is used as a starting material in the preparation of ethyl 2,2-dibromohexanoate, which is an important compound in various chemical reactions and applications.
Used in the Preparation of 2-mercaptohexanoic Acid Derivatives:
Ethyl 2-bromohexanoate can be converted into 2-mercaptohexanoic acid derivatives, which have various applications in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds.
Used in the Preparation of Chloroquinoxaline N-oxide:
Ethyl 2-bromohexanoate is used in the synthesis of chloroquinoxaline N-oxide, which is a compound with potential applications in various fields, such as pharmaceuticals and materials science.

InChI:InChI=1/C8H15BrO2/c1-3-5-6-7(9)8(10)11-4-2/h7H,3-6H2,1-2H3/t7-/m1/s1

Upstream product

• 142-61-0 Hexanoyl chloride 
• 142-62-1 hexanoic acid 
• 123-66-0 Ethyl hexanoate 
• 64-17-5 ethanol 
• 56-23-5 tetrachloromethane 
• 2985-32-2 butylmalonic acid monoethyl ester 
• 7726-95-6 bromine 
• 54971-26-5 2-bromohexanoyl bromide 
• 623-73-4 diazoacetic acid ethyl ester 
• 122-56-5 tributyl borane 

Downstream Products

• 1552-67-6 ethyl hex-2-enoate 
• 2396-83-0 ethyl hex-3-enoate 
• 52089-55-1 2-hydroxyhexanoic acid ethyl ester 
• 4447-54-5 ethyl 2-nitrohexanoate 
• 4134-14-9 ethyl 2-(diethoxyphosphoryl)hexanoate 
• 3462-35-9 2-Aethyl-3-butyl-2-phenyl-bernsteinsaeure-4-aethylester-1-nitril 
• 3462-36-0 3-Butyl-2-phenyl-2-propyl-bernsteinsaeure-4-aethylester-1-nitril 
• 63538-31-8 2-{4-[4-(1-Ethoxycarbonyl-pentyloxy)-phenoxy]-phenoxy}-hexanoic acid ethyl ester 
• 40843-43-4 4-(4-Chlorphenoxy)-α-phenoxy-capronsaeure-ethylester 
• 33559-27-2 2-(4-hydroxycarbamimidoyl-phenoxy)-hexanoic acid ethyl ester 
• 16584-05-7 1-ethylbenzotriazole 
• 115054-74-5 ethyl α-(benzotriazol-1-yl)hexanoate 
• 616-05-7 (R)-(+)-2-bromohexanoic acid 
• 91423-84-6 (2S)-2-bromohexanoic acid 

Relevant academic research and scientific papers

Spin adduct formation from lipophilic EMPO-derived spin traps with various oxygen- and carbon-centered radicals

Free radicals are involved in the onset of many diseases, therefore the availability of adequate spin traps is crucial to the identification and localization of free radical formation in biological systems. In recent studies several hydrophilic compounds of 2-ethoxycarbonyl-2-methyl-pyrroline-N-oxide (EMPO) have been found to form rather stable Superoxide spin adducts with half-lives up to twenty minutes at physiological pH. This is a major improvement over DMPO (t1/2 = ca. 45 s), and even over DEPMPO (t1/2 = ca. 14 min), the best commercially available spin trap for the unambiguous detection of superoxide radicals. In order to allow the detection of superoxide and also other radicals in lipid environment a series of more lipophilic derivatives of EMPO was synthesized and their structure unambiguously characterized by 1H and 13C NMR spectroscopy. In this way, six different compounds with a n-butyl group in position 5 and either an ethoxy- (EBPO), propoxy- (PBPO), iso-propoxy- (iPBPO), butoxy- (BBPO), sec-butoxy- (sBBPO) or tert-butoxycarbonyl group (tBBPO) in position 5 of the pyrroline ring were obtained and fully analytically characterized (NMR, IR). The stability of the superoxide adducts of all investigated spin traps were comparable with EMPO (t1/2 = ca. 8 min), except for the two compounds bearing an additional methyl group in position 3 or 4 of the pyrroline ring, 5-butyl-5-ethoxycarbonyl-3-methyl-pyrroline-N-oxide (BEMPO-3) and 5-butyl-5-ethoxycarbonyl-4-methyl-pyrroline-N-oxide (BEMPO-4), of which the superoxide adducts were stable for more than 30 min. Spin adducts of other carbon- and oxygen-centered radicals were also investigated.

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.