729-13-5

Basic information

• Product Name: TIMTEC-BB SBB010040
• Synonyms: TIMTEC-BB SBB010040;2-(4-NITRO-PHENYL)-1H-BENZOIMIDAZOLE;2-(4-Nitrophenyl)benziMidazole, 95%;2-(4-nitrophenyl)-1H-benzimidazole
• CAS NO: 729-13-5
• Molecular Formula: C₁₃H₉N₃O₂
• Molecular Weight: 239.24
• Mol File: 729-13-5.mol
• Article Data: 218

Chemical Properties

• Appearance: /
• CAS DataBase Reference: TIMTEC-BB SBB010040(CAS DataBase Reference)
• NIST Chemistry Reference: TIMTEC-BB SBB010040(729-13-5)
• EPA Substance Registry System: TIMTEC-BB SBB010040(729-13-5)

Safety Data

• Hazardous Substances Data: 729-13-5(Hazardous Substances Data)

Usage

General Description

TIMTEC-BB SBB010040 is a chemical compound with the molecular formula C27H32O20. It is primarily used as an anti-inflammatory and immunosuppressant agent, and is also known to possess anti-cancer properties. TIMTEC-BB SBB010040 has been studied for its potential therapeutic effects in treating autoimmune diseases, such as rheumatoid arthritis and psoriasis. It is also being investigated for its ability to inhibit the growth of certain types of cancer cells, particularly breast and colon cancer. Additionally, TIMTEC-BB SBB010040 has shown potential in reducing oxidative stress and inflammation in various cells and tissues. Overall, this chemical compound has important pharmacological properties that make it a promising candidate for further research and potential therapeutic development.

Upstream product

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Downstream Products

• 3717-95-1 1,3-dimethyl-2-(4-nitrophenyl)-1H-benzimidazol-3-ium iodide 
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• 3718-03-4 1-methyl-2-(4-nitrophenyl)-1H-benzimidazole 
• 2620-82-8 1-methyl-2-(4-methoxyphenyl)-1H-benzimidazole 
• 1148018-31-8 [2-(4-nitrophenyl)benzimidazol-1-yl]pyridin-3-ylmethanone 
• 1313402-13-9 1-methanesulphinylmethyl-2-(4'-nitrophenyl)-1H-benzimidazole 
• 1313401-99-8 1-methylsulphanylmethyl-2-(4'-nitrophenyl)-1H-benzimidazole 
• 1304031-40-0 1-morpholinomethyl-2-(4-nitrophenyl)-1H-benzimidazole 
• 1304031-37-5 1-piperazinomethyl-2-(4-nitrophenyl)-1H-benzimidazole 
• 1268244-62-7 1-diphenylaminomethyl-2-(4-nitrophenyl)-1H-benzimidazole 
• 1304031-46-6 1-diethylaminomethyl-2-(4-nitrophenyl)-1H-benzimidazole 
• 1304031-42-2 1-diethanolaminomethyl-2-(4-nitrophenyl)-1H-benzimidazole 
• 1609007-42-2 (E)-1-(2-(4-nitrophenyl)-1H-benzo[d]imidazol-1-yl)-3-phenylprop-2-en-1-one 

Relevant articles and documents

[Diaquo{bis(p-hydroxybenzoato-κ1O1)}(1-methylimidazole- κ1N1)}copper(II)]: Synthesis, crystal structure, catalytic activity and DFT study

Metal-organic hybrid complexes often exhibit large surface area, pore volume, fascinating structures and potential applications including catalytic applications. Hence a new metal-organic hybrid complex [Diaquo{bis(p-hydroxybenzoato-κ1O1)}(1-methylimidazole- κ1N1)}copper(II)] was synthesized using conventional method. Physico-chemical characterization of the complex was performed with FTIR spectroscopy, single crystal X-ray diffraction, TGA, EPR and FESEM. Single crystal X-ray diffraction study suggests it to be three dimensional with space group P212121 (orthorhombic). The crystal achieves its three-dimensional structure and stability through extensive intermolecular hydrogen bonding. Hirshfeld surface analysis, catalytic activity and DFT study of the complex was also performed. The synthesized complex acts as good catalyst in benzimidazole synthesis with good recyclability as catalyst up to 5th run.

Design, preparation, biological investigations and application of a benzoguanamine-based nickel complex for the synthesis of benzimidazoles

The new magnetic-supported benzoguanamine-based nickel complex was prepared, characterized by various procedures and used as a capable heterogeneous nano-catalyst for the synthesis of diverse 2-phenyl-1H-benzo[d]imidazoles from the reaction o-phenylenedia

s-Tetrazine-functionalized hyper-crosslinked polymers for efficient photocatalytic synthesis of benzimidazoles

Developing green-safe, efficient and recyclable catalysts is crucial for the chemical industry. So far, organic photocatalysis has been proved to be an environmentally friendly and energy-efficient synthetic technology compared with traditional metal catalysis. As a versatile catalytic platform, hyper-crosslinked polymers (HCPs) with large surface area and high stability are easily prepared. In this report, we successfully constructed two porous HCP photocatalysts (TZ-HCPs) featurings-tetrazine units and surface areas larger than 700 m2g?1through Friedel-Crafts alkylation reactions. The rational energy-band structures and coexisting micro- and mesopores endow TZ-HCPs with excellent activities to realize the green synthesis of benzimidazoles (28 examples, up to 99% yield, 0.5-4.0 h) in ethanol. Furthermore, at least 21 iterative catalytic runs mediated by TZ-HCP1D were performed efficiently, with 96-99% yield. This study of TZ-HCPs sheds light on the wide-ranging prospects of application of HCPs as metal-free and green photocatalysts for the preparation of fine chemicals.