95970-05-1

Basic information

• Product Name: 2,6-dibromo-4-methoxyaniline
• Synonyms: 2,6-dibromo-4-methoxyaniline;2,6-Dibromo-p-anisidine;6-dibroMo-4-MethoxybenzenaMine;2,6-DibroMo-4-Methoxy-phenylaMine;2,6-dibroMo-4-MethoxybenzenaMine;Benzenamine, 2,6-dibromo-4-methoxy-
• CAS NO: 95970-05-1
• Molecular Formula: C₇H₇Br₂NO
• Molecular Weight: 281
• Mol File: 95970-05-1.mol
• Article Data: 16

Chemical Properties

• Melting Point: 81-83℃
• Boiling Point: 293.6°C at 760 mmHg
• Flash Point: 131.4°C
• Appearance: /
• Density: 1.897
• Vapor Pressure: 0.00171mmHg at 25°C
• Refractive Index: 1.627
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• CAS DataBase Reference: 2,6-dibromo-4-methoxyaniline(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-dibromo-4-methoxyaniline(95970-05-1)
• EPA Substance Registry System: 2,6-dibromo-4-methoxyaniline(95970-05-1)

Safety Data

• Hazardous Substances Data: 95970-05-1(Hazardous Substances Data)

Usage

General Description

2,6-dibromo-4-methoxyaniline, also known as 2,6-dibromo-4-methoxybenzenamine, is a chemical compound with the molecular formula C7H7Br2NO. It is a substituted aniline derivative with two bromine atoms and one methoxy group attached to the benzene ring. It is commonly used in the synthesis of pharmaceuticals, dyes, and agrochemicals. The compound is a pale yellow to brown solid that is sparingly soluble in water but more soluble in organic solvents. It is considered to be a hazardous substance and should be handled and disposed of according to proper safety protocols. 2,6-dibromo-4-methoxyaniline is often used as an intermediate in the production of various products and is known for its antimicrobial and antioxidant properties.

InChI:InChI=1/C7H7Br2NO/c1-11-4-2-5(8)7(10)6(9)3-4/h2-3H,10H2,1H3

Upstream product

• 67-66-3 chloroform 
• 7726-95-6 bromine 
• 104-94-9 4-methoxy-aniline 
• 32338-02-6 2-bromo-4-methoxyaniline 

Downstream Products

• 32338-02-6 2-bromo-4-methoxyaniline 
• 201161-11-7 1,3-dibromo-2-iodo-5-methoxybenzene 
• 95970-06-2 2,3,6-tribromo-4-methoxyaniline 
• 1240480-30-1 2-amino-5-methoxy-1,3-benzenedicarboxylic acid 
• 30507-16-5 3-(4-methoxyphenyl)-2-methylquinazolin-4(3H)-one 

Relevant articles and documents

From Zn(II) to Cu(II) framework via single-crystal to single-crystal metathesis with superior gas uptake and heterogeneous catalytic properties

In this work, a Zn(II) framework, {[Zn2(L)4(H2O)4]·(7DMF)(7H2O)}n (1Zn), has been synthesized using a bent tetracarboxylic acid ligand (H4L). The structure of 1Zn contains [Zn2(COO)4] paddle-wheel secondary building units with axial sites occupied by water molecules. Interestingly, the isostructural Cu(II) framework {[Cu2(L)4(H2O)4]·(7DMF)(7H2O)}n (1Cu) has been obtained via single-crystal to single-crystal metathesis reaction. The activated 1Cu (denoted as a1Cu; a stands for activated) has open coordination sites. This species showed enhanced CO2 adsorption and heterogeneous catalytic properties for the Hantzsch coupling reaction involving condensation of an aldehyde with ethyl acetoacetate and ammonium acetate to produce 1,4-dihydropyridines, and three-component coupling of amines, aldehydes and alkynes to generate propargylic amines with high efficiency.

Multi-responsive metal-organic lantern cages in solution

Soluble copper-based M4L4 lantern-type metal-organic cages bearing internal amines were synthesized. The solution state integrity of the paramagnetic metal-organic cages was demonstrated using NMR, DLS, MS, and AFM spectroscopy. 1D s

Convergent total syntheses of the amaryllidaceae alkaloids lycoranine A, lycoranine B, and 2-methoxypratosine

The title alkaloids, 1, 2, and 3 respectively, have been prepared in a convergent manner by two related routes. The superior one involves C-H functionalization of the relevant 5-methoxyindole at C-7 using Hartwig's protocol and thus forming the correspond