107-09-5

Basic information

• Product Name: 2-bromoethylamine
• Synonyms: 2-bromoethylamine;BROMOETHANAMINE;EthanaMine, 2-broMo-;1-Amino-2-bromoethane
• CAS NO: 107-09-5
• Molecular Formula: C₂H₆BrN
• Molecular Weight: 123.97974
• EINECS: 203-461-8
• Mol File: 107-09-5.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 131.8°Cat760mmHg
• Flash Point: 33.5°C
• Appearance: /
• Density: 1.6017 (rough estimate)
• Vapor Pressure: 9.12mmHg at 25°C
• Refractive Index: 1.4800 (estimate)
• PKA: 7.75±0.10(Predicted)
• CAS DataBase Reference: 2-bromoethylamine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-bromoethylamine(107-09-5)
• EPA Substance Registry System: 2-bromoethylamine(107-09-5)

Safety Data

• Hazardous Substances Data: 107-09-5(Hazardous Substances Data)

Usage

General Description

2-Bromoethylamine is a chemical compound with the formula C2H6BrN. It is an organic compound with a bromine atom attached to a two carbon chain, featuring an amine group. 2-bromoethylamine is synthetically prepared and is used as an intermediate in the synthesis of various pharmaceuticals and organic compounds. 2-Bromoethylamine is known for its use in the production of anti-inflammatory and analgesic drugs and is also used in the study of neurochemistry and pharmacology. 2-bromoethylamine is a colorless liquid with a strong, ammonia-like odor, and it is classified as a hazardous substance. Additionally, 2-Bromoethylamine is known to be toxic if ingested, inhaled, or absorbed through the skin, and it should be handled with proper safety precautions.

InChI:InChI=1/C2H6BrN.BrH/c3-1-2-4;/h1-2,4H2;1H

Upstream product

• 574-98-1 2-(2-bromoethyl)isoindoline-1,3-dione 
• 45328-65-2 aziridine; hydrobromide 
• 141-43-5 ethanolamine 
• 98945-49-4 N-(2-bromoethyl)phthalimic acid 
• 10035-10-6 hydrogen bromide 
• 151-56-4 ethyleneimine 
• 21841-57-6 aziridine borane 
• 133056-80-1 2-(3-Hydroxypropyl)-4-(2'-hydroxyethylamino)phthalazin-1(2H)-one 

Downstream Products

• 5459-68-7 2-(N,N-dimethylamino)ethyl bromide 
• 101269-74-3 2,5-bis-(2-bromo-ethylamino)-terephthalic acid diethyl ester 
• 349137-21-9 4-methoxy-3-nitro-benzoic acid-(2-bromo-ethylamide) 
• 36517-93-8 2-propylsulfanylethylamine 
• 18542-42-2 (2-aminoethyl)methylsulfide 
• 24665-93-8 2-Imino-1,3-oxazolidin 
• 64-04-0 phenethylamine 
• 7452-78-0 ethyl N-(2-bromoethyl)carbamate 
• 102942-89-2 N-(4-Methylphenyl)-4,5-dihydro-2-thiazolamine 
• 27110-61-8 N-(2-Bromo-ethyl)-benzamide 
• 101374-10-1 N-methyl-N-m-tolyl-ethylenediamine 
• 53844-02-3 benzyl N-(2-bromoethyl)carbamate 
• 99857-46-2 N-(4-ethoxy-phenyl)-N'-(2-bromo-ethyl)-urea 
• 100711-91-9 N-(2-bromo-ethyl)-N'-[1]naphthyl-urea 

Related news

Absorption of Cr(VI) onto amino-modified titanate nanotubes using 2-bromoethylamine (cas 107-09-5) hydrobromide through SN2 reaction08/18/2019

Unlike the complex reaction of grafting amino groups using harmful organic solvents, we proposed an environmental friendly method for effective amino grafting on titanate nanotubes (TNTs) with 2-Bromoethylamine hydrobromide (2-Bh) through a two-step SN2 reaction in pure water solution. The amino...detailed

Relevant articles and documents

Kinetics and Mechanism of Alkaline Hydrolysis of N-(2-bromoethyl)phthalamic Acid

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Reversible Closure and Cleavage of the Aziridinium Ring by Nucleophilic Substitution: Solvent Effects

The kinetics of ring opening of aziridinium ion by chloride and bromide ions in DMSO-water mixtures have been studied and compared with previously reported data on the reverse reaction.Activation parameters indicate that the C-Hal bond in the transition state of the reaction develops to a minor extent.This assumption is corroborated by the bromide:chloride ratio.Correlations with Kamlet-Taft solvent parameters showed that both opening and closure of the aziridinium ring are characterized by a similar nucleophilic solvation term.Taking this fact into account we assume a considerable degree of ring formation in the transition state of the reaction under study.

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