594-51-4

Usage

Appearance

Colorless to pale yellow liquid The compound is a liquid with a color that ranges from colorless to pale yellow.

Odor

Strong, pungent It has a noticeable and irritating smell.

Usage

Reagent in organic synthesis It is commonly used as a reagent in the synthesis of organic compounds.

Applications

Production of pharmaceuticals and agrochemicals 2,3-dibromo-2-methylbutane is used in the manufacturing of various medicines and agricultural chemicals.

Industrial use

Preparation of derivatives for plastics, rubber, and other products It is used to create various derivatives that are used in the production of plastics, rubber, and other industrial products.

Flammability

Highly flammable The chemical is highly susceptible to catching fire and can pose a significant risk.

Health and environmental hazards

Potential hazard to human health and the environment Exposure to 2,3-dibromo-2-methylbutane can be harmful to both humans and the environment.

Handling and storage requirements

Strict requirements Proper handling and storage procedures must be followed to minimize risks associated with this chemical compound.

InChI:InChI=1/C5H10Br2/c1-4(6)5(2,3)7/h4H,1-3H3

Upstream product

• 513-35-9 2-methyl-but-2-ene 
• 15501-33-4 neopentyl iodide 
• 56-23-5 tetrachloromethane 
• 75-85-4 tert-Amyl alcohol 
• 7726-95-6 bromine 
• 7732-18-5 water 
• 1630-94-0 1,1-dimethylcyclopropane 
• 507-36-8 2-bromo-2-methylbutane 
• 594-36-5 2-methyl-2-butylchloride 
• 109318-01-6 2,2-dimethylpropane-1,1-diyl bis(trifluoromethanesulfonate) 
• 3712-44-5 2,2,2-tribromo-1,3,2-benzodioxaphosphole 
• 630-19-3 pivalaldehyde 
• 24443-15-0 1,3-dibromo-3-methylbutane 

Downstream Products

• 513-35-9 2-methyl-but-2-ene 
• 78-79-5 isoprene 
• 598-25-4 Dimethylallene 
• 563-80-4 3-methyl-butan-2-one 
• 5396-58-7 2-methyl-2,3-butanediol 
• 630-19-3 pivalaldehyde 
• 590-86-3 isovaleraldehyde 
• 54462-66-7 1,4-dibromo-2-methyl-butane 
• 26465-83-8 1,1-dimethyl-3-phenyl-1H-indene 
• 5076-19-7 trimethyloxirane 
• 10271-33-7 2-(2-benzoyl-phenyl)-2-methyl-propionic acid 
• 2938-98-9 2-methyl-1,4-butandiol 
• 10271-34-8 1-Acetoxy-1-phenyl-3-oxo-4,4-dimethyl-3,4-dihydro-1H-2-benzopyran 
• 858509-60-1 1,1-dimethyl-2-nitro-3-phenyl-indene 

Relevant academic research and scientific papers

Brominative Deoxygenation of Some Aldehydes and Ethers

Three aldehydes (4a-c) are transformed into 1,1-dibromides (6a-c) by 2,2,2-tribromo-2,2-dihydro-1,3,2-benzodioxaphosphole (2).This reagent (2) is also very active in the cleavage of ethers; its reactions may show some features of carbonium as well as of SN2 character.

Synthesis of 1,1-Dihaloalkanes

The reaction of 1,1-bistrifluoromethylsulfonyloxy-alkanes (2) with magnesium iodide in carbon disulphide at O deg C affords 1,1-diiodoalkanes (3-I) in good yields.No rearrangement products are observed.The reaction of 2 with magnesium bromide in carbon disulphide or titanium tetrachloride in dichloromethane yields either 1,1-dichloro- (3-Cl) or 1,1-dibromoalkanes (3-Br).Rearrangements products are formed from α-branched substrates.

Bromochlorination of Alkenes with Dichlorobromate (1-) ion. IV. Regiochemistry of Bromochlorinations of Alkenes with Molecular Bromine Chloride and Dichlorobromate (1-) Ion

The regioselectivity of the addition of molecular bromine chloride to alkenes is dependent on both the steric and electronic effects of the alkyl substituent.In contrast, the regioselectivity of the addition of dichlorobromate (1-) ion to alkenes is controlled mainly by the steric effect of the substituent.

One-pot Conversions of Amines into Olefins via Non-isolated Pyridinium Intermediates

Secondary alkyl primary amines are converted by the pyrylium salt (1) directly at 20 deg C into olefins via the corresponding secondary carbenium ions.Isomeric olefin mixtures are elucidated and result from carbenium ion rearrangements.

Palladium-Catalyzed Three Carbon Chain Extension Reactions with Acrolein Acetals. A Convenient Synthesis of Conjugated Dienals

A variety of vinylic halides has been found to react with acrolein or methacrolein acetals and amines with palladium catalysts to form 5-amino 3-enal acetals and/or dienal acetals.The reaction products yield 2,4-dienals on treatment with aqueous acids, in moderate to good yields.Crotonaldehyde dimethyl acetal also undergoes the reaction, but only in low yields. 3-Buten-2-one ethylene ketal reacted well under the same conditions, however, and Hofmann elimination and hydrolysis of the product amine gave (E,E)-3,5-heptadien-2-one in 90percent yield.