2,3,4,5-Tetrachloroaniline

Base Information

• Chemical Name: 2,3,4,5-Tetrachloroaniline
• CAS No.: 634-83-3
• Molecular Formula: C6H3 Cl4 N
• Molecular Weight: 230.909
• Hs Code.: 2921420090
• European Community (EC) Number: 211-216-1
• UNII: 55FY7XX7MH
• DSSTox Substance ID: DTXSID70212810
• Nikkaji Number: J1.712D
• Wikidata: Q83088014
• Mol file: 634-83-3.mol

Synonyms:2,3,4,5-tetrachloroaniline

Chemical Property of 2,3,4,5-Tetrachloroaniline

Chemical Property:

• Vapor Pressure: 0.000229mmHg at 25°C
• Melting Point: 118 °C
• Boiling Point: 325.5°C at 760 mmHg
• PKA: -0.10±0.10(Predicted)
• Flash Point: >100 °C
• PSA: 26.02000
• Density: 1.655g/cm³
• LogP: 4.46360
• Storage Temp.: 2-8°C
• XLogP3: 4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 230.899010
• Heavy Atom Count: 11
• Complexity: 143

Purity/Quality:

98%Min ^*data from raw suppliers

2,3,4,5-Tetrachloroaniline ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xn,N,F
• Hazard Codes: Xn,N,F
• Statements: 22-37/38-41-43-50/53-36-20/21/22-11
• Safety Statements: 26-36/37/39-60-61-36/37-16

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: C1=C(C(=C(C(=C1Cl)Cl)Cl)Cl)N
• Uses: 2,3,4,5-Tetrachloroaniline, is the metabolite of pentachloronitrobenzene (P237990), having fungicidal activities. It is also used as an intermediate for the synthesis of chlorinated compounds, such as polychlorinated biphenyls (PCBs).

Technology Process of 2,3,4,5-Tetrachloroaniline

There total 6 articles about 2,3,4,5-Tetrachloroaniline 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:

→ 2,3,4,5-tetrachloroaniline (634-83-3)

Guidance literature:

With alkali;

Reference yield:

2,3,4,5-tetrachloronitrobenzene (879-39-0) → 2,3,4,5-tetrachloroaniline (634-83-3)

Guidance literature:

With hydrogenchloride; tin;

Reference yield:

tetrachlorophthalamic acid (56113-42-9) → 2,3,4,5-tetrachloroaniline (634-83-3)

Guidance literature:

Multi-step reaction with 2 steps

1: NaOH-solution; alkaline sodium hypochlorite / Erwaermen auf 70-80grad

2: beim Erhitzen ueber den Schmelzpunkt

With sodium hydroxide; alkaline sodium hypochlorite;

upstream raw materials:

2,3,4,5-tetrachloronitrobenzene

3,4,5,6-tetrachloranthranilic acid

ethanol

1-(N-phenylcarbamoyl)piperidine

Downstream raw materials:

2,3,4,5-tetrachlorophenol

tetrachloro-2,3,4,5α-chloroacetanilide

4'-hydroxy-2,2',3,3',4,5,5'-heptachlorobiphenyl

2,2',3,4,4',5',6-heptachlorobiphenyl