94159-35-0

Usage

Halogenated organic compound

Contains a bromine atom 2,3-dihydroxypropyl bromoacetate is a halogenated organic compound as it contains a bromine atom in its structure.

Bromoacetate group

Presence of a bromine-substituted acetate group The compound has a bromoacetate group, which is a key functional group in its structure.

Two hydroxy groups

Attachment of two hydroxyl (-OH) groups 2,3-dihydroxypropyl bromoacetate has two hydroxy groups attached to its propyl chain, contributing to its reactivity and properties.

Propyl chain

Three-carbon backbone The compound features a propyl chain, which is a three-carbon backbone, to which the functional groups are attached.

Use as a reagent

Chemical synthesis and organic reactions 2,3-dihydroxypropyl bromoacetate is commonly used as a reagent in the preparation of various types of esters and other organic compounds.

Applications in industries

Pharmaceutical and agrochemical The compound is utilized in the pharmaceutical and agrochemical industries for the production of various products.

Potential intermediate

Production of other organic compounds 2,3-dihydroxypropyl bromoacetate is known to be a potential intermediate in the synthesis of other organic compounds, making it a versatile and important building block in organic chemistry.

InChI:InChI=1/C5H9BrO4/c6-1-5(9)10-3-4(8)2-7/h4,7-8H,1-3H2

Upstream product

• 925670-97-9 ((S)-2,2-dimethyl-1,3-dioxolan-4-yl)methyl 2-bromoacetate 
• 79-08-3 bromoacetic acid 
• 56-81-5 glycerol 

Relevant academic research and scientific papers

A method for preparing 2, 4 - dichlorophenoxyacetic acid (by machine translation)

The invention provides a 2, 4 - dichlorophenoxyacetic acid preparation method, comprises the following steps, first the polyol and a halogenated acetic acid to carry out the esterification reaction, to obtain halogenated acetate; then the above-mentioned step to obtain the halo acetate with 2, 4 - dichlorophen salt, to obtain 2, 4 - dichlorophenoxy ester; finally in the composite under the action of catalyst, obtained by the above-mentioned step 2, 4 - dichlorophenoxy ester hydrolytic reaction, to obtain 2, 4 - dichloro acid and polyol; the polyol C atoms is greater than or equal to 2 polyol. The invention adjusts the process route, from creative improvement on the basis of, the preparation method, the process is simple, mild condition, hydrolysis few by-products, the product has high purity, the conversion and yield higher, and intermediate halogenated acetate stable, suitable for large-scale industrial production. (by machine translation)

Synthesis of boron cluster lipids: Closo-dodecaborate as an alternative hydrophilic function of boronated liposomes for neutron capture therapy

(Chemical Equation Presented) We succeeded in the synthesis of the double-tailed boron cluster lipids 4a-c and 5a-c, which have a B 12H11S moiety as a hydrophilic function, by S-alkylation of B12H11SH (BSH) with bromoacetyl and chloroacetocarbamate derivatives of diacylglycerols for a liposomal boron delivery system on neutron capture therapy. Calcein encapsulation experiments revealed that the liposomes, prepared from the boron cluster lipid 4b, DMPC, PEG-DSPE, and cholesterol, are stable at 37°C in FBS solution for 24 h.