p-aminophenate anion

Base Information

• Chemical Name: p-aminophenate anion
• CAS No.: 19052-59-6
• Molecular Formula: C₆H₆NO
• Molecular Weight: 108.12
• Mol file: 19052-59-6.mol

Synonyms:p-aminophenate anion

Chemical Property of p-aminophenate anion

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of p-aminophenate anion

There total 12 articles about p-aminophenate anion 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-nitrophenol sodium salt (824-78-2) → p-aminophenate anion (19052-59-6)

Guidance literature:

With 1,3,5-tris(nicotinamidomethyl)-2,4,6-trimethylbenzene nitrate metallogel bed containing Ag nanoparticles; In water; dimethyl sulfoxide; at 20 ℃;

DOI:10.1002/chem.201404959

Reference yield:

p-aminophenol hydrochloride (51-78-5) → C12H9N2O2(1-) + p-aminophenate anion (19052-59-6)

Guidance literature:

Multi-step reaction with 5 steps

1: hydrogenchloride; sodium nitrite / water / 1 h

2: sodium azide / water; methanol / 1 h / -15 °C

3: tetramethyl ammoniumhydroxide / methanol

4: acetonitrile / 1.5 h / -27.5 °C / UV-irradiation

5: acetonitrile / 5 °C / UV-irradiation

With hydrogenchloride; sodium azide; tetramethyl ammoniumhydroxide; sodium nitrite; In methanol; water; acetonitrile;

DOI:10.1016/j.jphotochem.2013.12.008

Reference yield:

4-hydroxyphenyldiazonium chloride (1073-71-8,50909-74-5) → C12H9N2O2(1-) + p-aminophenate anion (19052-59-6)

Guidance literature:

Multi-step reaction with 4 steps

1: sodium azide / water; methanol / 1 h / -15 °C

2: tetramethyl ammoniumhydroxide / methanol

3: acetonitrile / 1.5 h / -27.5 °C / UV-irradiation

4: acetonitrile / 5 °C / UV-irradiation

With sodium azide; tetramethyl ammoniumhydroxide; In methanol; water; acetonitrile;

DOI:10.1016/j.jphotochem.2013.12.008

upstream raw materials:

p-aminophenoxyl radical

p-C₆H₄NH₂S^(1-)

C₆H₄OS^(2-)

p-aminophenol hydrochloride

Downstream raw materials:

p-benzyloxyaniline

p-aminophenoxyl radical

p-C₆H₄NH₂S^(1-)