699-11-6

Basic information

• Product Name: N-(2-bromoethyl)aniline
• Synonyms: N-(2-Bromoethyl)benzenamine
• CAS NO: 699-11-6
• Molecular Formula: C₈H₁₀BrN
• Molecular Weight: 200.0757
• EINECS: 211-827-3
• Mol File: 699-11-6.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 280°Cat760mmHg
• Flash Point: 123.2°C
• Appearance: /
• Density: 1.443g/cm³
• CAS DataBase Reference: N-(2-bromoethyl)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-bromoethyl)aniline(699-11-6)
• EPA Substance Registry System: N-(2-bromoethyl)aniline(699-11-6)

Safety Data

• Hazardous Substances Data: 699-11-6(Hazardous Substances Data)

Usage

General Description

N-(2-Bromoethyl)aniline is a chemical compound with the molecular formula C8H10BrN. It is an aromatic amine that contains a bromine atom and an ethyl group attached to the nitrogen atom. N-(2-Bromoethyl)aniline is commonly used in the synthesis of pharmaceuticals, dyes, and other organic compounds. It is a colorless to pale yellow liquid with a strong odor and is highly soluble in organic solvents such as alcohol and ether. N-(2-Bromoethyl)aniline is considered to be a hazardous substance and should be handled with care, as it can cause skin and eye irritation, and may be harmful if ingested or inhaled.

InChI:InChI=1/C8H10BrN/c9-6-7-10-8-4-2-1-3-5-8/h1-5,10H,6-7H2

Upstream product

• 124-38-9 carbon dioxide 
• 106-93-4 ethylene dibromide 
• 62-53-3 aniline 
• 41210-94-0 2-hydroxylethylphenylamine hydrochloride 
• 122-98-5 2-Anilinoethanol 

Downstream Products

• 1227813-16-2 N-(2-(2-iodophenoxy)ethyl)aniline 
• 1491141-21-9 C₁₄H₁₅N₅ 
• 174194-54-8 C₈H₁₀N₄ 
• 1450913-31-1 C₃₉H₃₉N₆O⁽¹⁺⁾ 
• 1450913-30-0 C₃₈H₃₇N₆⁽¹⁺⁾ 
• 1450913-19-5 C₃₈H₃₇N₆⁽¹⁺⁾ 
• 1450913-18-4 C₃₄H₃₅N₆⁽¹⁺⁾ 
• 1450913-17-3 C₃₄H₃₅N₆⁽¹⁺⁾ 
• 1450913-16-2 C₂₇H₂₇N₅O 
• 423719-93-1 N-phenyl-N,N',N'-tris(2-pyridylmethyl)ethane-1,2-diamine 
• 1450913-24-2 N¹-phenyl-N¹-(pyridin-2-ylmethyl)ethane-1,2-diamine 
• 1001197-80-3 7-methyl-1-phenylindoline 
• 753491-58-6 4-(2-oxo-3-phenyl-imidazolidin-1-yl)-benzoic acid ethyl ester 
• 905306-38-9 (2-diphenylphosphanyl-phenyl)-(2-phenylamino-ethyl)-carbamic acid tert-butyl ester 

Relevant articles and documents

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Cationic N-substituted aniline ionic liquid and preparation method thereof

The invention discloses a cationic N-substituted aniline ionic liquid, wherein an N-substituted aniline structure is contained in positive ions, and preferably, the structure of the cationic N-substituted aniline ionic liquid is shown as formula (I). A preparation method of the cationic N-substituted aniline ionic liquid comprises the following steps: firstly preparing N-phenylethanolamine hydrobromide, then preparing N-phenylethanolamine bromide from N-phenylethanolamine hydrobromide, and finally reacting N-phenylethanolamine bromide with compounds as shown in formulas (II-1) to (II-14) to obtain the cationic N-substituted aniline ionic liquid. The cationic N-substituted aniline ionic liquid has the properties and applications of common ionic liquid (such as serving as a reaction medium,an additive of a polymer material and the like), can be used as a monomer, can also be used as a reaction monomer to prepare ionic liquid polyaniline derivative through self oxidative polymerization or oxidative copolymerization with other monomers, and can also be combined with other polymerization means (such as free radical polymerization and the like) to prepare ionic liquid polyaniline derivatives and compounds of the ionic liquid polyaniline derivatives and other polymers.

Focused fluorescent probe library for metal cations and biological anions

A focused fluorescent probe library for metal cations was developed by combining metal chelators and picolinium/quinolinium moieties as combinatorial blocks connected through a styryl group. Furthermore, metal complexes derived from metal chelators having high binding affinities for metal cations were used to construct a focused probe library for phosphorylated biomolecules. More than 250 fluorescent probes were screened for identifying an ultraselective probe for dTTP.