615-83-8

Usage

Chemical Properties

clear colorless liquid

InChI:InChI=1/C7H13BrO2/c1-3-5-6(8)7(9)10-4-2/h6H,3-5H2,1-2H3/t6-/m1/s1

Upstream product

• 64-17-5 ethanol 
• 109-52-4 valeric acid 
• 33786-47-9 (E)-2-propyl-2-pentenoic acid 
• 83818-64-8 ((Z)-1-Chloro-pent-1-enylsulfanyl)-benzene 

Downstream Products

• 7463-34-5 ethyl (2E)-2-(hydroxyimino)pentanoate 
• 3462-31-5 *opt.-inakt. 3-Cyan-3-phenyl-2-propyl-valeriansaeure-aethylester 
• 63574-34-5 2-{4-[4-(1-Ethoxycarbonyl-butoxy)-phenoxy]-phenoxy}-pentanoic acid ethyl ester 
• 69461-35-4 N-(1-oxo-1-aethoxy-2-pentyl)-N-phenyl-N-trifluormethansulfonamid 
• 32884-99-4 2,3-Di-n-propyl-bernsteinsaeurediethylester 
• 816-26-2 ethyl 2-fluoropentanoate 
• 693288-49-2 2-diethylamino-pentan-1-ol 
• 35051-49-1 2-diethoxyphosphoryl-pentanoic acid ethyl ester 
• 97546-37-7 2-[2-(2-{2-[2-(1-Carboxy-butoxy)-phenoxy]-ethoxy}-ethoxy)-phenoxy]-pentanoic acid 
• 104273-60-1 2-(5-Benzoyl-1H-benzoimidazol-2-ylsulfanyl)-pentanoic acid ethyl ester 
• 85232-02-6 diethyl N-tert-butyloxycarbonylphosphoramidate 
• 85232-01-5 C₁₆H₃₂NO₇P 
• 97546-29-7 2-(2-{1-[2-(1-Carboxy-butoxy)-phenoxymethyl]-propoxy}-phenoxy)-pentanoic acid 
• 88795-76-0 ethyl ester of the 2-propyl-3-phenyl-2,3-epoxypropionic acid 

Relevant academic research and scientific papers

Process for preparing (E)-2-propyl-2-pentenoic acid and intermediate compounds

Composition consisting of a mixture of (E) and (Z) isomers of esters of general formula: STR1 in which R represents a C1 -C4 alkyl radical, containing at least 85% of (E) isomer. A process for preparing such a composition. The use of such a composition for preparing (E)-2-propyl-2-pentenoic acid of formula: STR2 and also its pharmaceutically acceptable salts.

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.

Alkyl alkanoate derivatives of substituted piperazine-diones and polymer compositions stabilized thereby

Alkyl alkanoate derivatives of substituted piperazinediones are stabilizers for synthetic polymeric materials normally subject to deterioration caused by ultraviolet light. The compounds may be formed by reacting a substituted piperazinedione with an acrylate or a crotonate, or reacting the alkali or alkaline earth salt of a substituted piperazine dione with a haloalkanoate. Polymeric compositions containing these stabilizers may also contain a hindered phenolic compound. A typical embodiment is n-octadecyl-β-(15{7,15-diazadispiro[5,1,5,3]hexadecane-14,16-dione}propionate.