5007-67-0

Basic information

• Product Name: 3.3'.4.4'-TETRA AMINOBENZOPHENONE
• Synonyms: 3,4,3',4'-Tetraaminobenzophenone;Bis(3,4-diaminophenyl)methanone;bis(3,4-Diaminophenyl)
• CAS NO: 5007-67-0
• Molecular Formula: C₁₃H₁₄N₄O
• Molecular Weight: 242.2765
• EINECS: 225-683-4
• Mol File: 5007-67-0.mol

Chemical Properties

• Melting Point: 216-218℃
• Boiling Point: 591.1±50.0 °C(Predicted)
• Appearance: /
• Density: 1.371
• PKA: 3.06±0.10(Predicted)
• CAS DataBase Reference: 3.3'.4.4'-TETRA AMINOBENZOPHENONE(CAS DataBase Reference)
• NIST Chemistry Reference: 3.3'.4.4'-TETRA AMINOBENZOPHENONE(5007-67-0)
• EPA Substance Registry System: 3.3'.4.4'-TETRA AMINOBENZOPHENONE(5007-67-0)

Safety Data

• Hazardous Substances Data: 5007-67-0(Hazardous Substances Data)

Usage

Uses

Used in Dye and Pigment Manufacturing:
3.3'.4.4'-TETRA AMINOBENZOPHENONE is used as a key component in the production of dyes and pigments for its ability to impart color and stability to these substances.
Used in Photoprotective Agents:
3.3'.4.4'-TETRA AMINOBENZOPHENONE is used as a photoprotective agent to safeguard materials from the damaging effects of ultraviolet radiation, thereby extending their lifespan and performance.
Used in Antistatic Agents:
3.3'.4.4'-TETRA AMINOBENZOPHENONE is used as an antistatic agent to reduce the buildup of static electricity on surfaces, which is crucial in industries such as electronics and textiles to prevent damage to sensitive components or materials.
Used in Electronic Device Production:
3.3'.4.4'-TETRA AMINOBENZOPHENONE is used as a material in the production of electronic devices, leveraging its stability and properties to enhance the performance and reliability of these devices.
Used in Biological Studies as a Fluorescent Probe:
3.3'.4.4'-TETRA AMINOBENZOPHENONE is used as a fluorescent probe in biological research, allowing for the visualization and tracking of cellular processes and components due to its fluorescent properties.
Used in Safety and Handling Procedures:
3.3'.4.4'-TETRA AMINOBENZOPHENONE is used in the development of safety and handling procedures due to its classification as a hazardous chemical, ensuring that workers and the environment are protected during its use and disposal.

Upstream product

• 108-86-1 bromobenzene 
• 90-98-2 4,4'-Dichlorobenzophenone 
• 87424-28-0 bis(4-bromo-3-nitrophenyl)methanone 
• 861781-57-9 4,4'-dibromo-3-nitro-benzophenone 
• 335015-51-5 4-bromo-3-nitrobenzoyl chloride 
• 7498-65-9 4,4'-dichloro-3,3'-dinitrobenzophenone 
• 19014-16-5 4,4'-diamino-3,3'-dinitrobenzophenone 

Downstream Products

• 40291-74-5 bis(dihydro-2-phenyl-1H-1,3,2-benzo diaza borolane-5-yl)ketone 
• 102342-72-3 2,2'-bis(carbomethoxyamino)-5,5'-dibenzimidazolyl ketone 
• 102342-72-3 C₁₉H₁₆N₆O₅ 

Relevant articles and documents

Studies in antiparasitic agents: Part 20 - Synthesis of probenzimidazoles, benzimidazoles and purimidobenzimidazoles as possible anthelmintics

A series of tetrasubstituted benzophenones (1-35) have been synthesized as probenzimidazoles.Some 2,5-disubstituted benzimidazoles (36-39 and 43-61) and pyrimidobenzimidazoles (40-42) have also been prepared.Of these compounds 4, 5, 15, 27, 29, 30, and 51 exhibit 100percent antihookworm activity against A. ceylanicum in hamsters at an oral dose of 250 mg/kg*3 while compounds 3, 4, 26-30 cause 100percent elimination of tapeworms, H. nana at a dose of 250 mg/kg.Compound 4 kills 90percent of the microfilariae of L. carinii at an intraperitoneal dose of 30 mg/kg*5.Another compound, 48 shows 6 4-78percent microfilaricidal and 38-62percent macrofilaricidal action against L. carinii and B. malayi at a dose of 50 mg/kg*5.

Synthesis and Anthelmintic Activity of Bisbenzimidazole-2-carbamates

The synthesis of bisbenzimidazole-2-carbamates (1-6) linked directly or by a one-atom bridge (CH2, CO, O, SO2, or S) at the 5 positions is described.Compound (4) shows interesting anthelmintic activity.