2-(2,4,6-Trinitroanilino)phenol

Base Information

• Chemical Name: 2-(2,4,6-Trinitroanilino)phenol
• CAS No.: 3163-19-7
• Molecular Formula: C12H8N4O7
• European Community (EC) Number: 654-012-1
• DSSTox Substance ID: DTXSID601288455
• Nikkaji Number: J1.429.473B
• Mol file: 3163-19-7.mol

Synonyms:2-(2,4,6-Trinitroanilino)phenol;3163-19-7;o-(2,4,6-Trinitroanilino)phenol;SCHEMBL11152164;SZULRCKZZUDMGB-UHFFFAOYSA-N;DTXSID601288455;2-(2,4,6-Trinitroanilino)phenol #;2-[(2,4,6-trinitrophenyl)amino]phenol

Chemical Property of 2-(2,4,6-Trinitroanilino)phenol

Chemical Property:

• XLogP3: 3.1
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 8
• Rotatable Bond Count: 2
• Exact Mass: 320.03929861
• Heavy Atom Count: 23
• Complexity: 448

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C(=C1)NC2=C(C=C(C=C2[N+](=O)[O-])[N+](=O)[O-])[N+](=O)[O-])O

Technology Process of 2-(2,4,6-Trinitroanilino)phenol

There total 7 articles about 2-(2,4,6-Trinitroanilino)phenol 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:

N-(2-hydroxy-phenyl)-N-picryl-acetamide → N-Picryl-2-aminophenol (3163-19-7)

Guidance literature:

With hydrogenchloride; acetic acid;

Reference yield:

2,4,6-trinitrochlorobenzene (88-88-0) + 2-amino-phenol (95-55-6) → N-Picryl-2-aminophenol (3163-19-7)

Guidance literature:

With benzene;

Reference yield:

2,4,6-trinitrochlorobenzene (88-88-0) → N-Picryl-2-aminophenol (3163-19-7)

Guidance literature:

Multi-step reaction with 2 steps

1: alcoholic KOH-solution

2: glacial acetic acid; concentrated hydrochloric acid

With hydrogenchloride; potassium hydroxide; acetic acid;

upstream raw materials:

2,4,6-trinitrochlorobenzene

2-amino-phenol

benzene

hydrogenchloride

Downstream raw materials:

1,3-Dinitro-phenoxazin

1,3,7-trinitro-10H-phenoxazine