430-91-1

Usage

Uses

Used in Synthetic Organic Chemistry:
BromoFluoroAcetamide is used as a reagent in synthetic organic chemistry for the preparation of a variety of organic compounds. Its unique structure and reactivity make it a valuable tool in the synthesis of complex organic molecules.
Used as a Biocidal Agent:
BromoFluoroAcetamide is used as a biocide for its potential antimicrobial properties. It has been studied for its ability to inhibit the growth of microorganisms, making it a candidate for applications in sanitization and disinfection processes.
Used in Environmental Control:
Due to its potential toxicity and environmental impact, BromoFluoroAcetamide is used in environmental control measures to ensure its release into the environment is carefully managed. This helps to avoid adverse effects on ecosystems and human health.

InChI:InChI=1/C2H3BrFNO/c3-1(4)2(5)6/h1H,(H2,5,6)

Upstream product

• 401-55-8 ethyl bromofluoroacetate 
• 1336-21-6 ammonium hydroxide 

Downstream Products

• 96449-14-8 bromofluoroacetonitrile 

Relevant academic research and scientific papers

A new approach to the synthesis of (Z)-2-fluoro-2-alkenals via Wittig-type carbonyl condensation reactions of 2-(fluoromethyl)-4,4,6-trimethyl-1,3-oxazine phosphonium bromide

We report here the transformation of aldehydes to their (Z)-α-fluoro-α,β-unsaturated aldehyde homologs by condensation with the phosphonium salt of the Meyer's oxazine obtained from bromofluoroacetonitrile. After methylation with trimethyloxonium tetrafluoroborate the quaternized oxazine is cleanly reduced to mostly Z 2-fluoro-2-alkenals by sodium borohydride at room temperature. This methodology is compatible with usual protecting groups and affords an efficient access to functionalized mostly Z 2-fluoro-2-alkenals derived from natural products and their corresponding (Z)-2-fluoro-2-alkenols.

Synthetic Studies for Novel Structure of α-Nitrogenously Functionalized α-Fluorocarboxylic Acids. Part 1. The First Synthesis and Reactions of N-Protected α-Fluoroglycines

The first synthesis of the N-protected α-fluoro-α-amino acid esters 12, 13, 21 and 22, and the corresponding acids 16 and 24, is described.Reaction of ethyl and t-butyl bromofluoroacetates 4 and 9 with di-t-butyl and dibenzyl iminodicarboxylate potassium

2-Fluoro-2-cyanoethenyl cyclopropane carboxylates as pesticides

Novel cyclopropanecarboxylates in all possible isomeric forms or mixtures thereof of the formula STR1 with a 1R,cis or 1R,trans structure and wherein X is a halogen, R is selected from the group consisting of (A) optionally unsaturated alkyl of 2 to 12 ca

Halonitriles, their preparation and use to make halopyridines

Novel halonitriles, e.g., 2,4-dichloro-2-fluoro-5,5-dimethoxy-4-methylpentanenitrile, method of preparation and use to make halopyridines, some of which are novel, e.g., 2-chloro-3-fluoro-5-methylpyridine. These compounds are intermediates in the preparation of pharmaceutical and agricultural products.