430-91-1

Basic information

• Product Name: BROMOFLUOROACETAMIDE
• Synonyms: 2-BROMO-2-FLUOROACETAMIDE;BROMOFLUOROACETAMIDE;Bromofluoroacetamide 98%;Bromofluoroacetamide98%;2-Bromo-2-fluoroacetamide 98%;2-Bromo-2-fluoroethanamide;2-Bromo-2-fluoroacetamide98%
• CAS NO: 430-91-1
• Molecular Formula: C2H3BrFNO
• Molecular Weight: 155.95
• Mol File: 430-91-1.mol
• Article Data: 4

Chemical Properties

• Melting Point: 44
• Boiling Point: 254.2°Cat760mmHg
• Flash Point: 107.5°C
• Appearance: /
• Density: 1.916g/cm³
• Vapor Pressure: 0.0175mmHg at 25°C
• Refractive Index: 1.47
• PKA: 13.18±0.50(Predicted)
• CAS DataBase Reference: BROMOFLUOROACETAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: BROMOFLUOROACETAMIDE(430-91-1)
• EPA Substance Registry System: BROMOFLUOROACETAMIDE(430-91-1)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38-36
• Safety Statements: 26-36/37/39
• HazardClass: IRRITANT
• Hazardous Substances Data: 430-91-1(Hazardous Substances Data)

Usage

General Description

BromoFluoroacetamide is a chemical compound with the molecular formula C2H3BrFNO. It is a brominated derivative of fluoroacetamide and is classified as a halogenated amide. BromoFluoroacetamide has been used in synthetic organic chemistry as a reagent in the preparation of a variety of organic compounds. It is also known for its potential use as a biocide and has been studied for its antimicrobial properties. However, its use is regulated due to its potential toxicity and environmental impact. BromoFluoroacetamide may pose health hazards if not handled and used properly, and its release into the environment must be carefully controlled to avoid adverse effects.

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 articles and documents

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.

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