24443-15-0

Usage

Uses

Used in Organic Synthesis:
1,3-Dibromo-3-methylbutane is utilized as a reagent in organic synthesis for the preparation of a wide range of chemicals. Its unique chemical structure allows it to participate in various reactions, making it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 1,3-dibromo-3-methylbutane serves as an intermediate in the manufacturing process of certain drugs. Its role in the synthesis of active pharmaceutical ingredients is crucial for the development of new medications.
Used in Agrochemical Production:
Similarly, in the agrochemical sector, 1,3-dibromo-3-methylbutane is employed as an intermediate for the production of various agrochemicals. Its contribution to the synthesis of effective crop protection agents is significant for agricultural productivity and pest management.
Safety Considerations:
It is important to handle 1,3-dibromo-3-methylbutane with care due to its classification as a hazardous material. Exposure to 1,3-DIBROMO-3-METHYLBUTANE may result in irritation to the respiratory system, skin, and eyes, necessitating proper safety measures during its use and storage.

InChI:InChI=1/C5H10Br2/c1-5(2,7)3-4-6/h3-4H2,1-2H3

Upstream product

• 10035-10-6 hydrogen bromide 
• 78-79-5 isoprene 
• 64-19-7 acetic acid 
• 201230-82-2 carbon monoxide 
• 536-74-3 phenylacetylene 
• 870-63-3 prenyl bromide 

Downstream Products

• 37746-17-1 1,5-dibromo-3,3-dimethylpentane 
• 22539-80-6 diethyl (3-methylbut-2-enyl)malonate 
• 110-93-0 6-Methyl-hept-5-en-2-on 
• 64-19-7 acetic acid 
• 2568-33-4 3-methyl-butane-1,3-diol 
• 594-51-4 2,3-dibromo-2-methylbutane 
• 78-79-5 isoprene 
• 64278-16-6 3,3-dimethyl-1,2,2-triphenyl-pyrrolidine 
• 64308-83-4 5,5-dimethyl-1,2-diphenyl-3,4,5,5a-tetrahydro-2H-benzo[c]azepine 
• 64278-01-9 [1-(1,1-Dimethyl-indan-5-yl)-1-phenyl-meth-(Z)-ylidene]-phenyl-amine 
• 64278-17-7 [(1,1-Dimethyl-indan-5-yl)-phenyl-methyl]-phenyl-amine 
• 154218-80-1 N-(3-methylbut-2-enyl)-4-phenylazetidine-2-one 
• 130400-97-4 [5-Bromo-2,2-dichloro-5-methyl-1-phenyl-hex-(Z)-ylidene]-isopropyl-amine 
• 563-45-1 3-Methyl-1-butene 

Relevant academic research and scientific papers

The Ni-mediated cyclocarbonylation of allyl halides and alkynes made catalytic. Evidence supporting the involvement of pseudoradical NiI species in the mechanism

We report here on a highly efficient catalytic method to synthesize intermolecularly the cyclopentane skeleton from starting products as simple as allyl halides, alkynes, and carbon monoxide under very mild reaction conditions by means of a substoichiomet