33170-72-8

Usage

Uses

Used in Organic Synthesis:
2-Bromo-1,1-dimethoxypropane is used as a reagent and intermediate for its ability to participate in various reactions, facilitating the formation of functional groups such as ethers and alkyl halides, which are essential in the synthesis of complex organic molecules.
Used in Pharmaceutical Preparation:
In the pharmaceutical industry, 2-Bromo-1,1-dimethoxypropane is utilized as a key component in the preparation of various drugs, contributing to the development of new medicinal compounds.
Used in Agrochemical Production:
2-Bromo-1,1-dimethoxypropane is also employed in the agrochemical sector, where it serves as an intermediate in the synthesis of chemicals used in agriculture to protect crops and enhance yields.
Used in Fine Chemicals Manufacturing:
2-Bromo-1,1-dimethoxypropane is used as a building block in the synthesis of fine chemicals, which are high-purity chemicals used in various applications, including research, diagnostics, and specialty manufacturing.
Used as a Protecting Agent for Alcohols:
In chemical reactions, 2-Bromo-1,1-dimethoxypropane is used to protect alcohols, preventing unwanted side reactions and ensuring the desired product is obtained with minimal byproducts.

InChI:InChI=1/C5H11BrO2/c1-4(6)5(7-2)8-3/h4-5H,1-3H3

Upstream product

• 4744-10-9 dimethoxypropane 
• 67-56-1 methanol 
• 123-38-6 propionaldehyde 
• 19967-57-8 bromo-2 propanal 
• 149-73-5 trimethyl orthoformate 

Downstream Products

• 60912-31-4 benzyl-(2,2-dimethoxy-1-methyl-ethyl)-amine 
• 1346702-05-3 6-{2-[4-(2,2-dimethoxy-1-methyl-ethoxy)phenyl]benzoxazol-6-yl}-5-ethyl-4,5-dihydro-2H-pyridazin-3-one 
• 1448317-31-4 1-(1,1-dimethoxypropan-2-yl)-1'-(4-methoxybenzyl)-N-(2-methyl-5-nitrophenyl)-1H,1'H-3,4'-bipyrazole-5-amine 
• 1216222-91-1 6-bromo-3-methylimidazo[1,2-a]pyridine 
• 19967-57-8 bromo-2 propanal 
• 49549-37-3 [7-chloro-5-(2-chloro-phenyl)-3H-benzo[e][1,4]diazepin-2-yl]-(2,2-dimethoxy-1-methyl-ethyl)-amine 
• 57390-38-2 2-amino-propionaldehyde dimethyl acetal 
• 79-10-7 acrylic acid 
• 14442-07-0 (2-bromo-2-phenyl-ethane-1,1-diyl)-bis-carbamic acid diethyl ester 
• 28434-48-2 2-methyl-5,6-diphenyl-2,3-dihydro-imidazo[2,1-b]thiazol-3-ol 

Relevant academic research and scientific papers

IMIDAZOLOPYRAZINE COMPOUNDS USEFUL FOR THE TREATMENT OF DEGENERATIVE AND INFLAMMATORY DISEASES

Novel imidazo[1,2-a]pyrazine compounds are disclosed that have a formula ( I ) represented by the following:The compounds may be prepared as pharmaceutical compositions, and may be used for the prevention and treatment of a variety of conditions in mammals including humans, including by way of non-limiting example, arthritis, inflammation, and others.

BROMINATION OF DIMETHYLACETALS WITH Br2-CHLOROTRIMETHYLSILANE-NaBr

α-Bromodimethylacetals are obtained in excellent yields by treating dimethylacetals with Br2-NaBr-chlorotrimethylsilane in CH3OH/CH3CN (2:1). The method is suitable for large scale preparation.

Ketene Chemistry 2. A General Procedure for the Synthesis of 2-Alkoxycyclopropanecarboxylic Esters and Acids Starting from Aldehydes and Ketene

Alkyl 3-alkoxy-4-bromocarboxylates are prepared by the Lewis acid-catalyzed reaction of α-bromoaldehyde acetals with ketene.Base-catalyzed cyclization of these intermediates affords 2-alkoxycyclopropanecarboxylic esters.

THE MUKAIYAMA REACTION OF KETENE BIS(TRIMETHYLSILYL)ACETALS WITH α-HALO ACETALS - A CONVENIENT BUTENOLIDE SYNTHESIS

Ketene bis(trimethylsilyl) acetals were reacted with α-halo acetals giving β-alkoxy-γ-halo acids which were converted to butenolides by reaction with equivalents of base.This constitutes a novel and short butenolide synthesis.

Method for the preparation of fragrances, and method for the preparation of perfume compositions

The invention relates to a method for the preparation of both known and novel fragrances and flavors, and in particular to the preparation and use of the novel fragrance compound, 2,6-nonadiene nitrile, and to a novel method for the preparation of 4-heptynal as the starting product for the preparation of the 2,6-nonadiene nitrile fragrance compound.