137469-70-6

Basic information

• Product Name: N-(5-BROMO-2-METHOXYBENZYL)-N-METHYLAMINE
• Synonyms: (5-bromo-2-methoxybenzyl)methylamine(SALTDATA: FREE);(5-bromo-2-methoxyphenyl)-N-methylmethanamine;5-bromo-2-methoxybenzyl)methylamine;5-bromo-2-methoxy-N-methyl-Benzenemethanamine
• CAS NO: 137469-70-6
• Molecular Formula: C₉H₁₂BrNO
• Molecular Weight: 230.1
• Mol File: 137469-70-6.mol

Chemical Properties

• Boiling Point: 271.9°Cat760mmHg
• Flash Point: 118.2°C
• Appearance: /
• Density: 1.343g/cm³
• Vapor Pressure: 0.00629mmHg at 25°C
• PKA: 9.25±0.10(Predicted)
• CAS DataBase Reference: N-(5-BROMO-2-METHOXYBENZYL)-N-METHYLAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: N-(5-BROMO-2-METHOXYBENZYL)-N-METHYLAMINE(137469-70-6)
• EPA Substance Registry System: N-(5-BROMO-2-METHOXYBENZYL)-N-METHYLAMINE(137469-70-6)

Safety Data

• Hazardous Substances Data: 137469-70-6(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
N-(5-BROMO-2-METHOXYBENZYL)-N-METHYLAMINE is used as a building block for the preparation of various pharmaceuticals and biologically active molecules. Its unique structure allows for the introduction of specific properties and functionality into organic molecules, making it a valuable tool in drug discovery and development.
Used in Research Chemicals:
N-(5-BROMO-2-METHOXYBENZYL)-N-METHYLAMINE is also used in the synthesis of potential drug candidates and research chemicals. Its versatility and reactivity make it a useful compound for exploring new chemical entities and advancing scientific research in the field of medicinal chemistry.

InChI:InChI=1/C9H12BrNO/c1-11-6-7-5-8(10)3-4-9(7)12-2/h3-5,11H,6H2,1-2H3/p+1

Upstream product

• 25016-01-7 5-bromo-2-methoxybenzaldehyde 
• 74-89-5 methylamine 

Downstream Products

• 137469-79-5 N-(3-bromo-6-methoxybenzyl)-N-methyl(phenylthio)acetamide 
• 137469-67-1 5-(2-acetylanilino)-1,4-dihydro-8-methoxy-2-methyl-4-phenylthio-3(2H)-isoquinolone 
• 137469-81-9 N-[5-(2-Acetyl-phenylamino)-2-methoxy-benzyl]-2-chloro-N-methyl-2-phenylsulfanyl-acetamide 
• 137469-66-0 5-methoxy-3,7-dimethyl-1-phenylthio-3,4-dihydrobenzo-<1,8>phenanthrolin-2(1H)-one 
• 137469-82-0 N-<3-(2-acetylanilino)-6-methoxybenzyl>-N-methyl(phenylsulphinyl)acetamide 
• 137469-80-8 N-<3-(2-acetylanilino)-6-methoxybenzyl>-N-methyl(phenylthio)acetamide 
• 137469-68-2 5-bromo-1,4-dihydro-8-methoxy-2-methyl-4-phenylthio-3(2H)-isoquinolone 
• 137469-73-9 8-methoxy-2-methyl-4-phenylthio-3(2H)-isoquinolone 

Relevant articles and documents

Synthesis of a Novel Tetracyclic Acridine. A Sulphoxide-based Route to the 1,2,3,4-Tetrahydrobenzophenanthroline Ring System

The ambit of the classical acridine synthesis, via acid-mediated cyclisation of 2-oxodiphenylamines, has been extended to include a sulphoxide-containing precursor.This adaption produced the tetracyclic system of 1 in a single step from 25.