4-Amino-3-(4-bromophenoxy)-pyridine

Base Information

• Chemical Name: 4-Amino-3-(4-bromophenoxy)-pyridine
• CAS No.: 509076-64-6
• Molecular Formula: C₁₁H₉BrN₂O
• Molecular Weight: 265.109
• DSSTox Substance ID: DTXSID80462743
• Wikidata: Q82287326
• Mol file: 509076-64-6.mol

Synonyms:4-amino-3-(4-bromophenoxy)-pyridine;509076-64-6;SCHEMBL4370679;DTXSID80462743;UVEHPPGZAFCCEJ-UHFFFAOYSA-N

Chemical Property of 4-Amino-3-(4-bromophenoxy)-pyridine

Chemical Property:

• XLogP3: 2.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 263.98983
• Heavy Atom Count: 15
• Complexity: 195

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=CC=C1OC2=C(C=CN=C2)N)Br

Technology Process of 4-Amino-3-(4-bromophenoxy)-pyridine

There total 3 articles about 4-Amino-3-(4-bromophenoxy)-pyridine 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:

4-nitro-3-(4-bromophenoxy)pyridine N-oxide (509076-63-5) → 4-amino-3-(4-bromophenoxy)pyridine (509076-64-6)

Guidance literature:

With iron; acetic acid; Heating;

DOI:10.1021/jm049480l

Reference yield:

3-Bromo-4-nitropyridine N-oxide (1678-49-5) → 4-amino-3-(4-bromophenoxy)pyridine (509076-64-6)

Guidance literature:

Multi-step reaction with 2 steps

1.1: aq. NaOH

1.2: 38 percent / acetonitrile / Heating

2.1: Fe; aq. acetic acid / Heating

With sodium hydroxide; iron; acetic acid;

DOI:10.1021/jm049480l

Reference yield:

4-bromo-phenol (106-41-2) → 4-amino-3-(4-bromophenoxy)pyridine (509076-64-6)

Guidance literature:

Multi-step reaction with 2 steps

1.1: aq. NaOH

1.2: 38 percent / acetonitrile / Heating

2.1: Fe; aq. acetic acid / Heating

With sodium hydroxide; iron; acetic acid;

DOI:10.1021/jm049480l

upstream raw materials:

4-nitro-3-(4-bromophenoxy)pyridine N-oxide

3-Bromo-4-nitropyridine N-oxide

4-bromo-phenol