600-05-5

Usage

Uses

Used in Chemical Analysis:
2,3-Dibromopropionic acid is used as a surrogate standard in the chemical shift imaging process during the analysis of multiple samples by multiplex sample NMR methodology. It serves as a reference compound to ensure accurate and reliable results in the analysis.
Used in Water Quality Assessment:
In the field of environmental chemistry, 2,3-Dibromopropionic acid is utilized as a surrogate standard for the extraction and determination of haloacetic acid in drinking water. This application aids in assessing the quality and safety of drinking water supplies.
Used in Gas Chromatography:
2,3-Dibromopropionic acid may also be employed as a surrogate standard for the quantification of haloacids in water samples using gas chromatography techniques. This application is crucial for accurate measurement and analysis of potentially harmful substances in water sources.

InChI:InChI=1/C3H4Br2O2/c4-1-2(5)3(6)7/h2H,1H2,(H,6,7)/p-1/t2-/m0/s1

Upstream product

• 5221-17-0 2,3-dibromopropanal 
• 96-13-9 2,3-Dibromopropan-1-ol 
• 10443-65-9 2-bromo-2-propenoic acid 
• 594-48-9 2,2-dibromopropionic acid 
• 107-13-1 acrylonitrile 
• 79-10-7 acrylic acid 
• 802294-64-0 propionic acid 
• 7726-95-6 bromine 
• 7664-93-9 sulfuric acid 
• 10035-10-6 hydrogen bromide 
• 7697-37-2 nitric acid 
• 2583-25-7 allylmalonic acid 
• 107790-74-9 2-methyl-3-(trimethylgermyl)propanoic acid 

Downstream Products

• 1729-67-5 Methyl 2,3-dibromopropionate 
• 3674-13-3 2,3-dibromopropionic acid ethyl ester 
• 6214-29-5 3-methoxy-2-propen-1-oic acid 
• 515-94-6 2,3-diaminopropanoic acid 
• 632-12-2 (RS)-isoserine 
• 473-81-4 glyceric acid 
• 473-81-4 (S)-glyceric acid 
• 17617-04-8 (+/-)-isocysteine 
• 10443-65-9 2-bromo-2-propenoic acid 
• 6220-25-3 1,2-dimercaptopropionic acid 
• 18791-02-1 2,3-dibromo-propionyl chloride 
• 79-10-7 acrylic acid 
• 859953-75-6 2,3-bis-benzylamino-propionic acid 
• 121388-33-8 2,3-dibromo-propionic acid cyclohexyl ester 

Relevant academic research and scientific papers

A 2, 3 - two bromine propionyl chlorides production process (by machine translation)

The present invention relates to the field of producing chemical products, especially 2, 3 - two bromine propionyl chlorides production field. 2. 3 - two bromine propionyl chlorides is an important chemical raw materials. Currently in production have different production process. The process flow includes: 1, addition; 2, distillation. (by machine translation)

An economical and convenient synthesis of vinyl sulfones

A general process for the efficient synthesis of vinyl sulfones has been developed using commercially available sulfinic acid sodium salts and dibromides. A variety of phenyl and methyl vinyl sulfones have been formed in good yields, in the absence of any catalyst. Georg Thieme Verlag Stuttgart.

Kinetic study of the Ce(III)-, Mn(II)-, or ferroin-catalyzed belousov-zhabotinsky reaction with allylmalonic acid

In a stirred batch experiment and under aerobic conditions, ferroin (Fe(phen)32+) behaves differently from Ce(III) or Mn(II) ion as a catalyst for the Belousov-Zhabotinsky (BZ) reaction with allylmalonic acid (AMA). The effects of bromate ion, AMA, metal-ion catalyst, and sulfuric acid on the oscillating pattern were investigated. The kinetics of the reaction of AMA with Ce(IV), Mn(III), or Fe(phen)33+ ion was studied under aerobic or anaerobic conditions. The order of reactivity of metal ions toward reaction with AMA is Fe(phen)33+ > Mn(III) > Ce(IV) under aerobic conditions whereas it is Mn(III) > Ce(IV) > Fe(phen)33+ under anaerobic conditions. Under aerobic or anaerobic conditions, the order of reactivity of RCH(CO2H)2 (R = H (MA), Me (MeMA), Et (EtMA), allyl (AMA), n-Bu (BuMA), Ph (PhMA), and Br (BrMA)) is PhMA > MA > BrMA > AMA > MeMA > EtMA > BuMA toward reaction with Ce(IV) ion and it is MA > PhMA > BrMA > MeMA > AMA > EtMA > BuMA toward reaction with Mn(III) ion. Under aerobic conditions, the order of reactivity of RCH(CO2H)2 toward reaction with Fe(phen)33+ ion is PhMA > BrMA > (MeMA, AMA) > (BuMA, EtMA) > MA. The experiment results are rationalized.

Reaction of (α-halogenoalkyl)thiiranes with nucleophilic reagents I. Reaction with morpholine

By means of deuterated compounds it was established that (chloromethyl)thiirane reacts with morpholine by a mechanism involving initial opening of the thiirane ring followed by recyclization.In the case of (bromomethyl)thiirane direct substitution of the bromine begins to compete with this mechanism. 2-Methyl-2-(chloromethyl)thiirane, 2,2-dimethyl-3-(chloromethyl)thiirane, and the diastereomeric (1-chloroethyl)thiiranes were synthesized, and their reactivity toward morpholine was studied.

Process for the preparation of 2,3-dibromopropionyl chloride

An improved process for the preparation of 2,3-dibromopropionyl chloride, which comprises brominating acrylic acid, adding iron powder or an iron salt to the resultant melt, chlorinating the dibromopropionic acid obtained, and removing the volatile components. The 2,3-dibromopropionyl chloride is obtained in high yield and purity and is an intermediate for synthesising in particular reactive dyes.

Synthesis and properties of germa-γ-lactones

Trialkylgermylpropanoic acids treated with 1 mole of bromine afford the monobromopropanoic acids, which are converted into the corresponding germa-γ-lactones in good yields by hydrolysis.The physical, chemical, and biological properties of these compounds are described.