50638-54-5

Basic information

• Product Name: N1,N1,2,6-TETRAMETHYL-4-BROMOANILINE
• Synonyms: (4-bromo-2,6-dimethyl-phenyl)-dimethyl-amine;BenzenaMine, 4-broMo-N,N,2,6-tetraMethyl-;N,N-Dimethyl-4-bromo-2,6-dimethylaniline;N,N-Dimethyl-4-bromo-2,6-xylidine;4-broMo-N,N,2,6-tetraMethylbenzenaMine;4-BROMO-N,N,2,6-TETRAMETHYLANILINE;N1,N1,2,6-TETRAMETHYL-4-BROMOANILINE;n-(4-bromo-2,6-dimethylphenyl)-n,n-dimethylamine
• CAS NO: 50638-54-5
• Molecular Formula: C₁₀H₁₄BrN
• Molecular Weight: 228.13
• Product Categories: Amines;Phenyls & Phenyl-Het;Phenyls & Phenyl-Het
• Mol File: 50638-54-5.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 270℃
• Flash Point: 117℃
• Appearance: /
• Density: 1.295
• Vapor Pressure: 0.00704mmHg at 25°C
• Refractive Index: 1.571
• CAS DataBase Reference: N1,N1,2,6-TETRAMETHYL-4-BROMOANILINE(CAS DataBase Reference)
• NIST Chemistry Reference: N1,N1,2,6-TETRAMETHYL-4-BROMOANILINE(50638-54-5)
• EPA Substance Registry System: N1,N1,2,6-TETRAMETHYL-4-BROMOANILINE(50638-54-5)

Safety Data

• Hazardous Substances Data: 50638-54-5(Hazardous Substances Data)

Usage

General Description

N1,N1,2,6-Tetramethyl-4-bromoaniline is a chemical compound with the molecular formula C10H15BrN. It is a substituted derivative of aniline, containing both methyl and bromine groups. N1,N1,2,6-TETRAMETHYL-4-BROMOANILINE is commonly used in the synthesis of various organic chemicals, pharmaceuticals, and agrochemicals. It is also used as an intermediate in the production of dyes and pigments. N1,N1,2,6-Tetramethyl-4-bromoaniline is a versatile building block in organic synthesis and has several industrial applications due to its unique chemical properties. However, it is important to handle and use this compound with care, as it may pose health and environmental risks if not properly managed.

InChI:InChI=1/C10H14BrN/c1-7-5-9(11)6-8(2)10(7)12(3)4/h5-6H,1-4H3

Upstream product

• 77-78-1 dimethyl sulfate 
• 50-00-0 formaldehyd 
• 64-18-6 formic acid 
• 24596-19-8 4-bromo-2,6-dimethylphenylamine 

Downstream Products

• 130948-54-8 bis(4-dimethylamino-3,5-dimethylphenyl)phosphine oxide 
• 1421275-80-0 C₂₈H₃₁N₅O₂ 
• 1421275-69-5 C₂₈H₂₉N₅O 
• 1421275-64-0 N,N,2,6-tetramethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenamine 
• 1616979-89-5 4,4'-(tert-butylphosphinediyl)bis(N,N,2,6-tetramethylaniline) 
• 1616980-18-7 C₂₄H₃₇N₂PSe 
• 930781-25-2 bis(4-dimethylamino-3,5-dimethylphenyl)phosphine-borane complex 
• 100618-20-0 4-dimethylamino-3,5-dimethyl-benzoic acid ethyl ester 
• 129430-90-6 N-Benzyl-(3R,4R)-(-)-3,4-bispyrrolidine 
• 129413-61-2 Bis<3,5-dimethyl-4-dimethylaminophenyl>phosphine 
• 129413-62-3 C₂₀H₂₉N₂OP 
• 87725-33-5 4-dimethylamino-3,5-dimethyl-benzoic acid 
• 40759-55-5 4,4'-bis-dimethylamino-3,5,3',5'-tetramethyl-benzophenone 

Relevant articles and documents

2-ARYL- AND 2-HETEROARYLTHIAZOLYL COMPOUNDS, METHODS FOR THEIR PREPARATION AND USE THEREOF

The present invention discloses fused bicyclic 2-aryl- or 2-heteroarylthiazolyl compounds and their pharmaceutically acceptable salts and esters thereof, which are useful for inhibiting the growth of cancerous cells, inhibiting human breast carcinoma tumo

Efficient asymmetric hydrogenation of (Z)-2-acetamidocinnamic acid catalyzed by the rhodium complex of modified n-Benzyl-(3R,4R)-3,4-bis(diphenylphosphino)pyrrolidine (degphos)

Modified Degphoses (R,R)-MOD-, XYL-Degphos) have been prepared and catalytic asymmetric hydrogenetion of (Z)-2-acetamidocinnamic acid was carried out with their rhodium(]) cationic complexes. The catalytic activities of the modified Degphoses were enhanced.