35911-17-2

Usage

Uses

1. Used in Organic Synthesis:
1,3-Dibromo-2-methyl-1-propene is used as a synthetic intermediate for the production of various organic compounds. Its reactivity allows for the formation of new chemical bonds, making it a valuable building block in the creation of complex molecules.
2. Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1,3-Dibromo-2-methyl-1-propene is used as a key component in the synthesis of certain drugs. Its unique structure and reactivity enable the development of new medications with potential therapeutic applications.
3. Used in Chemical Research:
1,3-Dibromo-2-methyl-1-propene is also utilized in chemical research as a model compound for studying various reaction mechanisms and exploring new synthetic pathways. This helps researchers gain a deeper understanding of organic chemistry and develop innovative methods for creating novel compounds.
4. Used in Material Science:
In the field of material science, 1,3-Dibromo-2-methyl-1-propene can be used to develop new materials with specific properties. Its incorporation into polymers or other materials can lead to the creation of materials with enhanced characteristics, such as improved stability or reactivity.

InChI:InChI=1/C4H6Br2/c1-4(2-5)3-6/h2H,3H2,1H3

Upstream product

• 3017-69-4 2-methyl-1-propenylbromide 
• 3100-04-7 Methylcyclopropen 
• 631-28-7 1,2,3-tribromo-2-methylpropane 
• 89089-31-6 3-bromo-2-methyl-prop-2-en-1-ol 

Downstream Products

• 3100-04-7 Methylcyclopropen 
• 725-02-0 Bis-<3-brom-2-methyl-prop-2-en-yl>-cyclohexylamin 
• 89089-31-6 3-bromo-2-methyl-prop-2-en-1-ol 
• 23230-96-8 2-t-Butoxymethyl-3-dimethylaminopropen 
• 84695-30-7 (Z)-3-bromo-2-methylprop-2-ene-1-ol 
• 84695-29-4 (E)-3-bromo-2-methyl-prop-2-en-1-ol 

Relevant academic research and scientific papers

Synthesis and biological activity of 2-aminoimidazole triazoles accessed by Suzuki-Miyaura cross-coupling

A pilot library of 2-aminoimidazole triazoles (2-AITs) was synthesized and assayed against Acinetobacter baumannii and methicillin-resistant Staphylococus aureus (MRSA). Results from these studies show that these new derivatives have improved biofilm dispersal activities as well as antibacterial properties against A. baumannii. With MRSA biofilms they are found to possess biofilm inhibition capabilities at low micromolar concentrations.

Stereoselective synthesis of 2-dienyl-substituted pyrrolidines using an η4-dienetricarbonyliron complex as the stereodirecting element: Elaboration to the pyrrolizidine skeleton

Primary amines react with keto-aldehyde functionality located in the side-chain of an η4-dienetricarbonyliron complex to provide the corresponding pyrrolidines in excellent diastereoselectivity. Two of the pyrrolidine products, 1i and 1k, have been elaborated into pyrrolizidines using a 1,5-C-H insertion and radical cyclization strategy, respectively.

Palladium-Catalyzed Syntheses of Conjugated Polyenes

Conjugated trienes have been prepared by the palladium-catalyzed reaction of vinylic bromides with 2,4-pentadienoic acid and its 3-methyl derivative, in the presence of triethylamine.Methyl (E)-3-bromo-2-methylpropenoate also forms conjugated trienes and in some instances also tetraenes when it is reacted with 1,3-dienes under similar conditions.Some loss of stereochemistry in the starting vinylic bromide or, more often, in the diene may occur in the rections presumably because equilibrating ?-allylic intermediates are involved.1,3,5-Hexatriene and 2 equiv of methyl (E)-3-bromo-3-methylpropenoate form orange-red dimethyl (E,E,E,E,E)-2,11-dimethyl-2,4,6,8,10-dodecapentaenedioate in modest yield.