23879-32-5

Basic information

• Product Name: BenzeneMethanaMine, N,N,3-triMethyl-
• Synonyms: BenzeneMethanaMine, N,N,3-triMethyl-;N,N,3-Trimethyl-benzenemethanamine
• CAS NO: 23879-32-5
• Molecular Formula: C₁₀H₁₅N
• Molecular Weight: 149.2328
• Mol File: 23879-32-5.mol
• Article Data: 16

Chemical Properties

• Appearance: /
• CAS DataBase Reference: BenzeneMethanaMine, N,N,3-triMethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: BenzeneMethanaMine, N,N,3-triMethyl-(23879-32-5)
• EPA Substance Registry System: BenzeneMethanaMine, N,N,3-triMethyl-(23879-32-5)

Safety Data

• Hazardous Substances Data: 23879-32-5(Hazardous Substances Data)

Usage

Description

BenzeneMethanaMine, N,N,3-triMethyl-, also known as Trimethylaniline, is a chemical compound with the molecular formula C9H13N. It is a colorless liquid with a faint aromatic odor and is highly flammable. BenzeneMethanaMine, N,N,3-triMethylis commonly used as a component in the production of dyes, pigments, and pharmaceuticals. It is important to handle this compound with caution, as it can be harmful if inhaled or absorbed through the skin. BenzeneMethanaMine, N,N,3-triMethylis classified as a hazardous substance and should be stored and handled according to safety regulations.

Uses

Used in Dye Production:
BenzeneMethanaMine, N,N,3-triMethylis used as a key component in the production of dyes, contributing to the development of various colorants for different applications.
Used in Pigment Production:
BenzeneMethanaMine, N,N,3-triMethylis also utilized in the production of pigments, which are essential for coloring various materials and products.
Used in Pharmaceutical Industry:
BenzeneMethanaMine, N,N,3-triMethylis used as a raw material in the manufacturing of pharmaceuticals, playing a crucial role in the development of various medications.

Upstream product

• 100-97-0 hexamethylenetetramine 
• 620-13-3 1-bromomethyl-3-methyl-benzene 
• 50-00-0 formaldehyd 
• 100-81-2 3-methyl-benzenemethanamine 
• 506-59-2 N,N-dimethylammonium chloride 
• 620-23-5 m-tolyl aldehyde 
• 114762-93-5 Ir{C₆H₃(CH₂N(CH₃)2)(CH₃)}(C₈H₁₂) 
• 114762-90-2 Ir{C₆H₃(CH₂N(CH₃)2)(CH₃)}(C₈H₁₂) 
• 124-38-9 carbon dioxide 
• 39180-84-2 N-methyl-1-(m-tolyl)methanamine 
• 67-56-1 methanol 
• 620-22-4 3-Methylbenzonitrile 
• 126799-82-4 1-(azidomethyl)-3-methylbenzene 
• 124-40-3 dimethyl amine 

Downstream Products

• 27561-28-0 3,N,N-Trimethyl-2-neopentylbenzylamin 
• 167031-64-3 Hg(C₆H₃(CH₃)-5-CH₂NMe₂-2)2 
• 1192229-87-0 3-methylbenzyldimethylamine borane 
• 1259324-52-1 N-(tert-butoxycarbonylmethyl)-N,N-dimethyl-N-(3-methylbenzyl)ammonium bromide 
• 1258839-86-9 ethyl 2-((dimethylamino)methyl)-4-methylbenzoate 
• 1349171-43-2 N,N-dimethyl-1-[5-methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanamine 
• 621-36-3 m-methylphenylacetic acid 

Relevant articles and documents

Palladium-Catalyzed Reductive Aminocarbonylation of Benzylammonium Triflates with o-Nitrobenzaldehydes for the Synthesis of 3-Arylquinolin-2(1 H)-ones

A palladium-catalyzed straightforward procedure for the synthesis of 3-arylquinolin-2(1H)-ones has been developed. The synthesis proceeds through a palladium-catalyzed reductive aminocarbonylation reaction of benzylic ammonium triflates with o-nitrobenzaldehydes, and a wide range of 3-arylquinolin-2(1H)-ones was obtained in moderate to good yields with very good functional group compatibility.

Cu2O-catalyzed C–S coupling of quaternary ammonium salts and sodium alkane-/arene-sulfinates

A new protocol for the synthesis of (enantioenriched) benzylic sulfones via the Cu2O-catalyzed C–S bond cross coupling of alkane-/arene-sulfinates and (enantioenriched) benzylic quaternary ammonium salts has been developed. The product benzylic sulfones were obtained in good to high yields (75–96%). Chiral arylmethyl sulfones with high enantiomeric excess (90–94% ee) were also synthesized in the presence of Cu2O and 1,1′-bis-(diphenylphosphino)ferrocene (dppf).

Electrochemical Dehydrogenative Imidation of N-Methyl-Substituted Benzylamines with Phthalimides for the Direct Synthesis of Phthalimide-Protected gem-Diamines

A general and green electrochemical dehydrogenative method for the imidation of N-methyl benzylamines with phthalimides with excellent regioselectivities is reported for the first time. This operationally simple method offers a valuable tool to obtain str