4-Bromo-2-ethoxyaniline

Base Information

Chemical Name:4-Bromo-2-ethoxyaniline
CAS No.:57279-73-9
Molecular Formula:C₈H₁₀BrNO
Molecular Weight:216.077
Hs Code.:
European Community (EC) Number:863-701-8
DSSTox Substance ID:DTXSID80574057
Wikidata:Q82462948

Synonyms:4-Bromo-2-ethoxyaniline;57279-73-9;4-bromo-2-ethoxybenzenamine;4-Bromo-2-ethoxy-aniline;SCHEMBL3856079;DTXSID80574057;FRYQWMDMRFFGRO-UHFFFAOYSA-N;MFCD12547811;AKOS014677724;AS-36365;EN300-109667;Z1259175664

Suppliers and Price of 4-Bromo-2-ethoxyaniline

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 2 raw suppliers

Chemical Property of 4-Bromo-2-ethoxyaniline

Chemical Property:

XLogP3:2.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:214.99458
Heavy Atom Count:11
Complexity:121

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC1=C(C=CC(=C1)Br)N

Technology Process of 4-Bromo-2-ethoxyaniline

There total 4 articles about 4-Bromo-2-ethoxyaniline 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: 96.0%

: 57279-70-6
4-bromo-2-ethoxy-1-nitro-benzene

: 57279-73-9
4-bromo-2-ethoxy-aniline

Guidance literature:: With iron; acetic acid; In ethanol; water; for 1.5h; Heating / reflux;

Reference yield:

: 321-23-3
4-bromo-2-fluoronitrobenzene

: 57279-73-9
4-bromo-2-ethoxy-aniline

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium hydride / tetrahydrofuran; mineral oil / 0.25 h / 0 °C / Inert atmosphere

1.2: 18 h / 0 - 20 °C

2.1: tin(ll) chloride / ethanol / 2 h / 70 °C

With sodium hydride; tin(ll) chloride; In tetrahydrofuran; ethanol; mineral oil;