600-30-6

Usage

Uses

Used in Agricultural Industry:
2,3-Dibromobutyric Acid is used as a key compound in the preparation of nematocidal alkenanilides for the agricultural industry. These alkenanilides are effective in controlling and eliminating nematodes, which are parasitic roundworms that can cause severe damage to crops and plants. By using 2,3-Dibromobutyric Acid in the synthesis of these nematocides, farmers can protect their crops from the harmful effects of nematode infestations, leading to increased crop yields and improved agricultural productivity.
Used in Chemical Synthesis:
In the field of chemical synthesis, 2,3-Dibromobutyric Acid serves as an important building block for the creation of various organic compounds. Its unique chemical structure allows it to be used in the synthesis of a wide range of molecules, including pharmaceuticals, agrochemicals, and other specialty chemicals. The versatility of 2,3-Dibromobutyric Acid makes it a valuable asset in the development of new and innovative products across various industries.
Used in Research and Development:
2,3-Dibromobutyric Acid is also utilized in research and development laboratories for the study of its chemical properties and potential applications. Scientists and researchers can use 2,3-DIBROMOBUTYRIC ACID to explore new reaction pathways, develop novel synthetic methods, and investigate its potential as a precursor to other valuable chemicals. The use of 2,3-Dibromobutyric Acid in research can lead to the discovery of new compounds and applications, further expanding its utility in various fields.

InChI:InChI=1/C4H6Br2O2/c1-2(5)3(6)4(7)8/h2-3H,1H3,(H,7,8)/p-1/t2-,3-/m1/s1

Upstream product

• 3724-65-0 2-butenoic acid 
• 4786-20-3 crotononitrile 
• 7726-95-6 bromine 
• 590-93-2 2-Butynoic acid 
• 503-64-0 (Z)-but-2-enoic acid 
• 36297-22-0 (E)-2-bromo-2-butenoic acid 
• 5405-34-5 (Z)-2-bromobut-2-enoic acid 
• 600-30-6 erythro-2,3-dibromobutanoic acid 
• 10035-10-6 hydrogen bromide 
• 107-93-7 (E)-but-2-enoic acid 
• 75-15-0 carbon disulfide 
• 56-23-5 tetrachloromethane 
• 4021-75-4 rac-(2R,3S)-2,3-dibromobutan-1-ol 
• 50553-14-5 2,3-dibromo-butyraldehyde 

Downstream Products

• 590-14-7 1-bromo-1-propene 
• 27243-23-8 α-bromocrotonic acid 
• 590-13-6 (Z)-1-propenyl bromide 
• 590-15-8 trans-2-propenyl bromide 
• 93501-09-8 α,β-Dibromohydrocrotonanilide 
• 3724-65-0 2-butenoic acid 
• 107-93-7 (E)-but-2-enoic acid 
• 103385-15-5 (±)-2,3-diphenylbutanoic acid 
• 590-93-2 2-Butynoic acid 
• 5469-24-9 methyl 2,3-dibromobutyrate 
• 600-30-6 (R,S/S,R)-α,β-dibromobutyric acid 
• 609-11-0 (+/-)-erythro-2,3-dibromo-butyric acid ethyl ester 
• 5350-86-7 anti-2,3-Diphenylbutanoic acid 
• 10035-10-6 hydrogen bromide 

Relevant academic research and scientific papers

Carbene-catalyzed LUMO activation of alkyne esters for access to functional pyridines

A carbene-catalyzed LUMO activation of α,β-unsaturated alkyne esters is reported. This catalytic process allows for effective reactions of alkyne esters with enamides to synthesize functional pyridines via simple protocols. A previously unexplored unsaturated alkyne acyl azolium intermediate is involved in the key step of the reaction.

α-Bromo-β,γ-unsaturated ketenes for the synthesis of α-benzylamino-β,γ-unsaturated acids

The synthesis of α-benzylamino-β,γ-unsaturated acids has been developed starting from α-bromo-α,β-unsaturated chlorides. Via treatment of the acyl chlorides with (R)-pantolactone in the presence of TEA, the in situ formation of the deconjugated ketenes and their direct transformation into chiral esters was performed. The substitution of bromine with benzylamine, followed by acid hydrolysis, allowed to us obtain enantiomerically enriched α-benzylamino-β,γ-unsaturated acids.

Iodide-catalysed cyclization of unsaturated N-chloroamines: A new way to synthesise 3-chloropiperidines

Tetrabutylammonium iodide is a very efficient catalyst for the cyclization of unsaturated N-chloroamines. The catalysis seems to proceed through N-iodoamine intermediates, which act as a source of iodonium ions. Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.

Synthesis of the Substituted Z-1-Bromo-1-alkenes and Arylacetylenes from 2,3-Dibromocarboxylic Acids

Stereoselectivity was studied of simultaneous debromination-decarboxylation of dibrominated cinnamic and acrylic acids. The best selectivity in formation of Z-vinyl bromides was achieved with the use of organic nitrogen bases. The 1-bromo-1-alkenes were converted into the corresponding acetylenes.

Nematicidal alkenanilides

A method is described for the control of nematodes in agricultural crops which comprises applying to the situs of infestation a nematicidal composition containing as active ingredient a compound of the formula STR1 wherein R1 and R2 are hydrogen, lower alkyl, or halogen, X is hydrogen or halogen, n is 1 or 2, Y is hydrogen, lower alkyl, halogen, trifluoromethyl, lower alkoxy, lower alkylthio, and nitro when n is 1, and halogen when n is 2, with the proviso that at least 1 of R1, R2, and X must be halogen. Preparation of active ingredient compounds is described, and nematicidal utility of compositions is exemplified.

A New Route for the Synthesis of Coumarins, Thiacoumarins and Carbostyrils

3-Arylcarbostyrils, coumarins and thiacoumarins (3) have been prepared from the respective β-aryl-α-bromodihydrocinnamoyl derivatives (2) by treatment with AlCl3.The β,β-diarylacrylic acid derivatives (4) and (9), obtained from 2, on reaction with AlCl3 afford 4-arylcarbostyrils (5) 6-methyl-4-phenylthiacoumarin (10) respectively.However the oxygen analogs (11) give 3,3-diphenyl-1-indanone (12)