101251-11-0

Basic information

• Product Name: (3-BroMo-4-Methyl-phenyl)-Methyl-aMine
• Synonyms: (3-BroMo-4-Methyl-phenyl)-Methyl-aMine;3-BroMo-N,4-diMethylaniline;3-bromo-N,4-dimethylbenzenamine
• CAS NO: 101251-11-0
• Molecular Formula: C₈H₁₀BrN
• Molecular Weight: 200.0757
• Mol File: 101251-11-0.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (3-BroMo-4-Methyl-phenyl)-Methyl-aMine(CAS DataBase Reference)
• NIST Chemistry Reference: (3-BroMo-4-Methyl-phenyl)-Methyl-aMine(101251-11-0)
• EPA Substance Registry System: (3-BroMo-4-Methyl-phenyl)-Methyl-aMine(101251-11-0)

Safety Data

• Hazardous Substances Data: 101251-11-0(Hazardous Substances Data)

Usage

General Description

(3-Bromo-4-Methyl-phenyl)-Methyl-aMine, also known as 4-methyl-3-bromobenzylamine, is a compound with the chemical formula C8H10BrN. It is an organic compound with a phenyl ring substituted with a bromine atom and a methyl group, as well as an amine group attached to the phenyl ring. (3-BroMo-4-Methyl-phenyl)-Methyl-aMine is commonly used in the synthesis of various pharmaceuticals and organic compounds. It is also used as a building block in the production of agrochemicals and biologically active molecules. Due to its versatile reactivity, it is widely utilized in chemical research and manufacturing processes.

Upstream product

• 67-56-1 methanol 
• 7745-91-7 3-bromo-4-methylaniline 
• 515813-02-2 tert-butyl (3-bromo-4-methylphenyl)carbamate 
• 77-78-1 dimethyl sulfate 
• 40371-61-7 N-(3-bromo-4-methyl-phenyl)acetamide 
• 74-88-4 methyl iodide 
• 53104-16-8 3-bromo-N,N,4-trimethylaniline 
• 877064-95-4 tert-butyl (3-bromo-4-methylphenyl)(methyl)carbamate 

Downstream Products

• 55270-47-8 5-methoxy-2-picoline 

Relevant articles and documents

Photodriven Photocatalyst/Metal-Free Direct C-C/C-N Bond Formation: Synthesis of Indoles via EDA Complexes

The photodriven direct C-C/C-N bond formation initiated by electron donor-acceptor (EDA) complexes for the synthesis of indoles has been accomplished via [3+2] annulations of secondary arylamines with alkynes using IC4F9 as oxidants in the absence of any photocatalysts and metals. This green transformation exhibits the advantages of operational simplicity, good functional tolerances, and mild reaction conditions. The in situ generated EDA complexes derived from arylamines with alkynes were characterized by UV-vis absorption spectrometry and NMR titration experiments.

Highly Efficient Binuclear Copper-catalyzed Oxidation of N,N-Dimethylanilines with O2

A binuclear copper-salicylate complex, [Cu(Sal)2(NCMe)]2 (Sal=salicylate), was found to be an active catalyst for the oxidation of N,N-dimethylanilines by O2, affording the corresponding N-methyl-N-phenylformamides as major products. The reactions were carried out with a O2 balloon and the S/C (substrate/catalyst ratio) of the model reaction could be up to 1×105, providing a practical and highly efficient catalytic protocol for accessing N-methyl-N-phenylformamides.

NOVEL BIAROMATIC COMPOUNDS THAT ACTIVATE PPAR TYPE RECEPTORS, AND USE THEREOF IN COSMETIC OR PHARMACEUTICAL COMPOSITIONS

The invention relates to novel biaromatic compounds that correspond to the general formula (I) and also to the method for preparing them, and to their use in pharmaceutical compositions for use in human or veterinary medicine (in dermatology, and also in the field of cardiovascular diseases, immune diseases and/or lipid metabolism-related diseases), or alternatively in cosmetic compositions.