2,4-Dichloro-N-hydroxyaniline

Base Information

• Chemical Name: 2,4-Dichloro-N-hydroxyaniline
• CAS No.: 43192-10-5
• Molecular Formula: C6H5Cl2NO
• Molecular Weight: 178.018
• Hs Code.: 2928000090
• European Community (EC) Number: 256-135-2
• DSSTox Substance ID: DTXSID50195773
• Nikkaji Number: J319.915K
• Wikidata: Q83068830
• Mol file: 43192-10-5.mol

Synonyms:2,4-Dichloro-N-hydroxyaniline;43192-10-5;EINECS 256-135-2;SCHEMBL11045353;DTXSID50195773;2,4-Dichloro-N-hydroxybenzenamine;N-(2,4-dichlorophenyl)-hydroxylamine

Chemical Property of 2,4-Dichloro-N-hydroxyaniline

Chemical Property:

• Vapor Pressure: 0.0023mmHg at 25°C
• Boiling Point: 276.5°Cat760mmHg
• Flash Point: 121°C
• PSA: 32.26000
• Density: 1.564g/cm³
• LogP: 2.86750
• XLogP3: 2.7
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 176.9748192
• Heavy Atom Count: 10
• Complexity: 112

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=C1Cl)Cl)NO

Technology Process of 2,4-Dichloro-N-hydroxyaniline

There total 2 articles about 2,4-Dichloro-N-hydroxyaniline 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:

2,4-dichloronitrobenzene (611-06-3) → hydroxylamine 2,4-dichloroaniline (43192-10-5)

Guidance literature:

With sodium hydrogensulfide; calcium chloride; benzene; weiteres Reagens: Wasser;

Reference yield:

→ hydroxylamine 2,4-dichloroaniline (43192-10-5)

Guidance literature:

/BRN= 2689905/;

Reference yield:

hydroxylamine 2,4-dichloroaniline (43192-10-5) → C6H4Cl2N2O2*H3N

Guidance literature:

With n-Butyl nitrite; ammonia; In diethyl ether; at 0 ℃; Yield given;

DOI:10.1080/00304949809355306

upstream raw materials:

2,4-dichloronitrobenzene

Downstream raw materials:

2,4-dichloro-1-nitrosobenzene

2,2',4,4'-tetrachloroazoxybenzene

[N-(2,4-Dichloro-phenyl)aminooxymethyl]-phenyl-carbamic acid methyl ester