38256-93-8

Basic information

• Product Name: N-(2-METHOXYETHYL)METHYLAMINE
• Synonyms: N-(METHOXYETHYL)METHYLAMINE;N-(2-METHOXYETHYL)METHYLAMINE;2-METHOXY-N-METHYL-1-ETHANAMINE;N-METHYL-2-METHOXYETHYLAMINE;1-Methoxy-2-(methylamino)ethane;Methyl(2-methoxyethyl)amine;N-(2-Methoxyethyl)-N-methylamine;N-Methyl-2-methoxyethanamine
• CAS NO: 38256-93-8
• Molecular Formula: C₄H₁₁NO
• Molecular Weight: 89.14
• Mol File: 38256-93-8.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 96 °C
• Flash Point: 1℃
• Appearance: /
• Density: 0.83
• Vapor Pressure: 113mmHg at 25°C
• Refractive Index: n20/D1.401
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• PKA: 9.52±0.10(Predicted)
• CAS DataBase Reference: N-(2-METHOXYETHYL)METHYLAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-METHOXYETHYL)METHYLAMINE(38256-93-8)
• EPA Substance Registry System: N-(2-METHOXYETHYL)METHYLAMINE(38256-93-8)

Safety Data

• Hazard Codes: Xi,Xn,F
• Statements: 11-34-43-41-37/38-22
• Safety Statements: 26-36/37/39
• RIDADR: 2734
• WGK Germany: 3
• HazardClass: IRRITANT
• PackingGroup: Ⅱ
• Hazardous Substances Data: 38256-93-8(Hazardous Substances Data)

Usage

General Description

N-(2-Methoxyethyl)methylamine is an organic chemical compound with the formula C4H11NO. It is a clear, colorless liquid with a faint, amine-like odor. N-(2-METHOXYETHYL)METHYLAMINE is commonly used as a building block in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. It is also used as a solvent and as an intermediate in the production of surfactants and detergents. N-(2-Methoxyethyl)methylamine is considered to be a hazardous substance and should be handled with care, as it can cause irritation to the skin, eyes, and respiratory system. Additionally, it is important to store and handle this compound in a well-ventilated area and to use appropriate personal protective equipment. Overall, N-(2-Methoxyethyl)methylamine plays a crucial role in the production of various chemicals and should be handled with caution due to its potential health hazards.

InChI:InChI=1/C4H11NO/c1-5-3-4-6-2/h5H,3-4H2,1-2H3

Upstream product

• 383868-51-7 N-(4-benzyloxy-7-morpholin-4-yl-benzothiazol-2-yl)-4-chloromethyl-benzamide 
• 88021-33-4 Trifluoro-methanesulfonate(2-methoxy-ethyl)-methyl-[2-methyl-prop-(E)-ylidene]-ammonium; 
• 141-43-5 ethanolamine 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 127944-62-1 benzyl (2R)-2-benzyl-3-<<(2-methoxyethyl)methylamino>carbonyl>propionate 
• 147238-87-7 Carbonic acid benzyl ester 2,6-dimethoxy-4-((5R,5aR,8aR,9S)-9-{2-[(2-methoxy-ethyl)-methyl-amino]-ethyl}-6-oxo-5,5a,6,8,8a,9-hexahydro-furo[3',4':6,7]naphtho[2,3-d][1,3]dioxol-5-yl)-phenyl ester 
• 737765-19-4 4-amino-6-(2,4-dichloro-phenyl)-2-[(2-methoxy-ethyl)-methyl-amino]-pyrimidine-5-carbonitrile 
• 819810-89-4 2-[2-ethyl-3,5-dihydroxy-6-(4-methoxybenzoyl)phenyl]-N-(2-methoxyethyl)-N-methylacetamide 
• 473547-15-8 {4-chloro-5-[(2-methoxy-ethyl)-methyl-amino]-2-nitro-phenyl}-carbamic acid tert.-butyl ester 
• 508238-45-7 2-(2-Furyl)-5-(3-methoxypropylamino)-8-(4-phenylpiperazin-1-ylmethyl)[1,2,4]triazolo[1,5-c]pyrimidine 
• 1048636-68-5 4,6-di-tert-butyl-2-([(2'-methoxyethyl)methylamino]methyl)phenol 
• 1224893-55-3 (8S)-N-(2-methoxyethyl)-N,2,3-trimethyl-8-(2-methylphenyl)-3,6,7,8-tetrahydrochromeno[7,8-d]imidazole-5-carboxamide 
• 1303527-29-8 C₂₃H₃₀ClN₃OS*ClH 
• 1339046-77-3 N₁-(2-methoxy-ethyl)-N₁-methyl-4-nitro-benzene-1,3-diamine 

Relevant articles and documents

Benzothiazole derivatives with activity as adenosine receptor ligands

The present invention relates to substituted benzothiazole derivitives and to their pharmaceutically acceptable salts useful for the treatment of diseases related to the adenosine receptor.

Schiff's Bases as Intermediates in the Hydrolytic Decomposition of 2-Alkyl-3-methyl-1,3-oxazolidines in Aqueous Acid

The kinetics for the hydrolysis of 2-alkyl-3-methyl-1,3-oxazolidines have been examined spectrophotometrically in acidic solutions.The decomposition of the substrates to 2-methylaminoethanol and the corresponding aldehydes have been shown to proceed via stable intermediates which are kinetically and u.v.-spectroscopically very similar to the acyclic cationic Schiff's base derived from isobutyraldehyde and 2-methoxyethylmethylamine.The mechanisms for the formation and breakdown of the Schiff's base intermediate are discussed on the basis of pH-rate profiles, activation parameters, salt effects, and solvent deuterium isotope effects.