2,3,4-Tribromo-6-methoxyaniline

Base Information

Chemical Name:2,3,4-Tribromo-6-methoxyaniline
CAS No.:95970-04-0
Molecular Formula:C7H6Br3NO
Molecular Weight:359.84100
Hs Code.:
DSSTox Substance ID:DTXSID201320190
ChEMBL ID:CHEMBL1481123

Synonyms:2,3,4-tribromo-6-methoxyaniline;Tribromaminoanisole;MLS001029708;CHEMBL1481123;DTXSID201320190;HMS2803I03;STK526847;AKOS005460231;2,3,4-Tribromo-6-methoxy-phenylamine;95970-04-0;SMR000427047

Suppliers and Price of 2,3,4-Tribromo-6-methoxyaniline

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 2,3,4-Tribromo-6-methoxyaniline

Chemical Property:

Melting Point:102 °C (acetic acid)
PSA：35.25000
LogP:4.14610
XLogP3:3.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:358.79790
Heavy Atom Count:12
Complexity:158

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC1=CC(=C(C(=C1N)Br)Br)Br

Technology Process of 2,3,4-Tribromo-6-methoxyaniline

There total 1 articles about 2,3,4-Tribromo-6-methoxyaniline which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 52.4%

: 90-04-0
2-methoxy-phenylamine

: 95970-04-0
2-Amino-3,4,5-tribromoanisole

Guidance literature:: With bromine; In acetic acid; at 20 - 25 ℃; for 3h;

Reference yield:

: 95970-04-0
2-Amino-3,4,5-tribromoanisole

: 6161-61-1
2,3,4,5-tetrabromoanisole

Guidance literature:: With copper(I) bromide; sulfuric acid; hydrogen bromide; sodium nitrite; Yield given. Multistep reaction; 1.) acetic acid, 0 deg C, 30 min, 2.) 0 deg C, 30 min, 3.) from 0 deg C, to 100 deg C, 1.5 h;;

Reference yield:

: 95970-04-0
2-Amino-3,4,5-tribromoanisole

: 73557-60-5
3,4,5-tribromo-anisole

Guidance literature:: With ethanol; sulfuric acid; sodium nitrite; Yield given. Multistep reaction; 1.) 0 deg C, 2.) 0 deg C, 15 min, 3.) heating to 80 deg C, 1 h;;