32315-92-7

Basic information

• Product Name: (2-CHLORO-ETHYL)-METHYL-AMINE
• Synonyms: (2-CHLORO-ETHYL)-METHYL-AMINE;2-chloro-N-methyl-ethanamine;2-(Methylamino)ethyl chloride;(2-chloroethyl)methylamine(SALTDATA: FREE);EthanaMine, 2-chloro-N-Methyl-
• CAS NO: 32315-92-7
• Molecular Formula: C₃H₈ClN
• Molecular Weight: 93.55532
• Mol File: 32315-92-7.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 110.3°Cat760mmHg
• Flash Point: 20.5°C
• Appearance: /
• Density: 0.952g/cm³
• Vapor Pressure: 23.8mmHg at 25°C
• Refractive Index: 1.41
• PKA: 8.75±0.10(Predicted)
• CAS DataBase Reference: (2-CHLORO-ETHYL)-METHYL-AMINE(CAS DataBase Reference)
• NIST Chemistry Reference: (2-CHLORO-ETHYL)-METHYL-AMINE(32315-92-7)
• EPA Substance Registry System: (2-CHLORO-ETHYL)-METHYL-AMINE(32315-92-7)

Safety Data

• Hazardous Substances Data: 32315-92-7(Hazardous Substances Data)

Usage

General Description

(2-Chloro-Ethyl)-Methyl-Amine is a chemical compound that belongs to the class of organic compounds known as haloamines which contain a halogen atom attached to an amine group. As the name suggests, this chemical has two main components - a 2-chloroethyl part and a methylamine part. The physical characteristics of the chemical vary, based on how it is stored or the substances it may be mixed with. It has various application in the chemical industry, and it’s used as a building block in the synthetic process of many chemical compounds. However, its concentrated or large-scale use needs careful handling and storage, because of potential health hazards: it is a known irritant and can cause damage to eyes, skin, and respiratory tract. Its safety and potential effects on the environment are also subjects of study and regulation in the chemical industry.

InChI:InChI=1/C3H8ClN/c1-5-3-2-4/h5H,2-3H2,1H3

Upstream product

• 109-83-1 (2-hydroxyethyl)(methyl)amine 
• 91418-07-4 chloro(ethylsulfanyl)acetylene 
• 56424-15-8 Butyl chloroethynyl sulfide 
• 66566-80-1 chloro(propylthio)acetylene 

Downstream Products

• 128696-32-2 [2-(ethanesulfonyl)ethyl](methyl)amine 
• 59127-74-1 5-methylamino-pentan-2-one 
• 142-25-6 N,N',N'-trimethylenediamine 
• 110-70-3 N,N`-dimethylethylenediamine 
• 743460-48-2 biphenyl-2-ylcarbamic acid 1-[2-(methylamino)ethyl]piperidin-4-yl ester 
• 220074-38-4 1,1-dimethylethyl N-(2-chloroethyl)-N-methylcarbamate 
• 20477-19-4 ethyl-(2-phenylphosphanyl-ethyl)-amine 
• 104-79-0 N,N-diethyl-N'-methylethane-1,2-diamine 
• 57375-54-9 N-<3-(N-methyl-N-(2-chlorethyl)carbamoyloxy)phenyl>-carbaminsaeure-isopropylester 
• 24701-51-7 demexiptiline 
• 111-37-5 N-methyl-N'-ethylethane-1,2-diamine 

Relevant articles and documents

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CYCLIN-DEPENDENT KINASE INHIBITORS

Described herein are compounds and their pharmaceutically acceptable salts, pharmaceutical compositions thereof, methods of treatment, and medical uses. The compounds described herein are modulators of cyclin-dependent kinases, and are useful in the treatment or alleviation of protein kinase associated disorders, including cancer, infectious diseases, autoimmune diseases, or cardiovascular diseases.

First multipurpose task specific ionic liquid: Designing and synthesis of novel dimethyl formamide-like ionic liquid and its applications as a green solvent alternative to dimethyl formamide dependent reactions

A novel imidazole based task specific ionic liquid with dimethyl formamide (DMF) functionality has been designed and synthesized. The proposed dimethyl formamide like task specific can be used as a green alternative solvent-cum-organocatalyst for wide range of organic reactions which essentially depend on DMF. Dimethyl formamide as a solvent, due to its inherited structural features is found to affect the outcome of many reactions. Some of DMF-dependent reactions are investigated in its ionic liquid version with encouraging results. DMFlike ionic liquid acts both as a green reaction media and recyclable organocatalyst. Main advantages include easy reaction procedure, short reaction duration, easy work up and moreover the wide scope applications.