123158-75-8

Basic information

• Product Name: 4-Chloro-2-iodo-6-nitro-phenylaMine
• Synonyms: 4-Chloro-2-iodo-6-nitro-phenylaMine;4-Chloro-2-iodo-6-nitroaniline
• CAS NO: 123158-75-8
• Molecular Formula: C₆H₄ClIN₂O₂
• Molecular Weight: 298.46563
• EINECS: -0
• Mol File: 123158-75-8.mol
• Article Data: 15

Chemical Properties

• Melting Point: 137-138 °C
• Boiling Point: 355.7±42.0 °C(Predicted)
• Appearance: /
• Density: 2.169±0.06 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• PKA: -3.20±0.25(Predicted)
• CAS DataBase Reference: 4-Chloro-2-iodo-6-nitro-phenylaMine(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Chloro-2-iodo-6-nitro-phenylaMine(123158-75-8)
• EPA Substance Registry System: 4-Chloro-2-iodo-6-nitro-phenylaMine(123158-75-8)

Safety Data

• Hazardous Substances Data: 123158-75-8(Hazardous Substances Data)

Upstream product

• 89-63-4 4-Chloro-2-nitroaniline 
• 64-19-7 acetic acid 
• 88-74-4 2-nitro-aniline 

Downstream Products

• 123158-76-9 1-chloro-3-iodo-5-nitrobenzene 
• 83171-49-7 3-chloro-5-iodoaniline 
• 153505-43-2 4-chloro-6-iodo-1.2-phenylenediamine 
• 1120334-15-7 5-chloro-7-nitro-3-phenyl-2-trimethylsilyl-1H-indole 
• 1180556-79-9 5-chloro-2-cyclohex-1-enyl-1H-indol-7-ylamine 
• 1180556-78-8 5-chloro-2-(3-chlorophenyl)-7-nitro-1H-indole 
• 1174672-63-9 C₈H₃ClF₃IN₂O₃ 
• 1120334-14-6 5-chloro-3-phenyl-7-nitro-1H-indole 

Relevant articles and documents

Pseudo-octahedral nickel(ii) complexes of strongly absorbing benzannulated pincer-type amido ligands: ligand-based redox and non-Aufbau electronic behaviour

The synthesis, structures and electronic characterization of three strongly coloured, pseudo-octahedral Ni(ii) complexes supported by redox-active diarylamido ligands featuring benzannulated N-heterocyclic donor arms are reported. The S = 1 paramagnets ea

NCBSI/KI: A Reagent System for Iodination of Aromatics through in Situ Generation of I-Cl

In situ iodine monochloride (I-Cl) generation followed by iodination of aromatics using NCBSI/KI system has been developed. The NCBSI reagent requires no activation due to longer bond length, lower bond dissociation energy, and higher absolute charge density on nitrogen. The system is adequate for mono- and diiodination of a wide range of moderate to highly activated arenes with good yield and purity. Moreover, the precursor N-(benzenesulfonyl)benzenesulfonamide can be recovered and transformed to NCBSI, making the protocol eco-friendly and cost-effective.

As cell necrosis inhibitors of the indole compounds (by machine translation)

The invention relates to chemical formula (1) indole compounds, or its pharmaceutically acceptable salt or isomer, and in containing the same as the characteristic, as an active ingredient for the prevention or treatment of cell necrosis and its associated disease composition and method of manufacturing. (by machine translation)