66314-77-0

Basic information

• Product Name: 3-broMo-2,4-diMethylaniline
• Synonyms: 3-broMo-2,4-diMethylaniline;3-Bromo-2,4-dimethylbenzenamine
• CAS NO: 66314-77-0
• Molecular Formula: C₈H₁₀BrN
• Molecular Weight: 200.0757
• Mol File: 66314-77-0.mol
• Article Data: 5

Chemical Properties

• Melting Point: 47-47.5 °C(Solv: methanol (67-56-1); water (7732-18-5))
• Boiling Point: 271.9±35.0 °C(Predicted)
• Appearance: /
• Density: 1.424±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 3.81±0.10(Predicted)
• CAS DataBase Reference: 3-broMo-2,4-diMethylaniline(CAS DataBase Reference)
• NIST Chemistry Reference: 3-broMo-2,4-diMethylaniline(66314-77-0)
• EPA Substance Registry System: 3-broMo-2,4-diMethylaniline(66314-77-0)

Safety Data

• Hazardous Substances Data: 66314-77-0(Hazardous Substances Data)

Usage

General Description

3-Bromo-2,4-dimethylaniline is a chemical compound with the molecular formula C8H10BrN. It is a substituted aniline with a bromine atom in the 3-position and two methyl groups in the 2- and 4-positions. 3-broMo-2,4-diMethylaniline is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It can also be used as a dye intermediate and in the production of polymer additives. 3-Bromo-2,4-dimethylaniline is a colorless to pale yellow liquid with a strong odor, and it is important to handle it with care as it can be harmful if ingested or inhaled.

Upstream product

• 576-22-7 2-Bromo-m-xylene 
• 69383-59-1 1-bromo-2,4-dimethyl-5-nitro-benzene 
• 60956-25-4 2-bromo-1,3-dimethyl-4-nitrobenzene 

Downstream Products

• 1056963-13-3 2,4-dimethyl-3-(pyrrolidin-1-yl)aniline 
• 1438436-02-2 N-(3-bromo-2,4-dimethylphenyl)phthalimide 
• 66314-79-2 3'-Brom-2,2-dichloro-2',4'-dimethylbenzoylacetanilid 
• 66314-78-1 3'-Brom-2',4'-dimethylbenzoylacetanilid 
• 3606-00-6 1-(3-bromo-2,4-dimethyl-phenyl)-piperazine 
• 74571-81-6 3-bromo-2,4-dimethylphenol 
• 926922-40-9 4-bromo-5-methyl-1H-indazole 

Relevant articles and documents

An N-Fluorinated Imide for Practical Catalytic Imidations

Catalytic imidation using NFSI as the nitrogen source has become an emerging tool for oxidative carbon-nitrogen bond formation. However, the less than ideal benzenesulfonimide moiety is incorporated into products, severely detracting its synthetic value.

Novel N9-arenethenyl purines as potent dual Src/Abl tyrosine kinase inhibitors

Novel N9-arenethenyl purines, optimized potent dual Src/Abl tyrosine kinase inhibitors, are described. The key structural feature is a trans vinyl linkage at N9 on the purine core which projects hydrophobic substituents into the sele

Phenylenediamine urotensin-II receptor antagonists and CCR-9 antagonists

The present invention relates to urotensin II receptor antagonists, CCR-9 antagonists, pharmaceutical compositions containing them and their use.