22868-35-5

Basic information

• Product Name: OTAVA-BB 1325766
• Synonyms: 2-(3-CHLOROPHENYL)-1H-1,3-BENZODIAZOLE;2-(3-CHLOROPHENYL)BENZIMIDAZOLE;OTAVA-BB 1325766;2-(3-Chloro-phenyl)-1H-benzoimidazole
• CAS NO: 22868-35-5
• Molecular Formula: C₁₃H₉ClN₂
• Molecular Weight: 228.681
• Mol File: 22868-35-5.mol
• Article Data: 97

Chemical Properties

• Boiling Point: 432.1°C at 760 mmHg
• Flash Point: 247.6°C
• Appearance: /Solid
• Density: 1.326g/cm³
• Vapor Pressure: 1.14E-07mmHg at 25°C
• Refractive Index: 1.693
• CAS DataBase Reference: OTAVA-BB 1325766(CAS DataBase Reference)
• NIST Chemistry Reference: OTAVA-BB 1325766(22868-35-5)
• EPA Substance Registry System: OTAVA-BB 1325766(22868-35-5)

Safety Data

• Hazardous Substances Data: 22868-35-5(Hazardous Substances Data)

Usage

Description

OTAVA-BB 1325766 is a heterocyclic chemical compound with a molecular formula of C20H18N4O4S2, featuring both sulfur and nitrogen atoms in its structure. It belongs to the class of sulfonamides, which are known for their use in the development of pharmaceuticals such as antibiotics and diuretics. Although the specific role and function of OTAVA-BB 1325766 are not clearly defined, its chemical structure indicates potential pharmacological activities. Further research and testing are necessary to determine its properties and applications comprehensively.

Uses

Used in Pharmaceutical Development:
OTAVA-BB 1325766 is used as a chemical compound in the pharmaceutical industry for its potential role in the development of new drugs. Its sulfonamide structure suggests that it may contribute to the creation of antibiotics or diuretics, which are essential in treating various medical conditions.
Used in Research and Testing:
In the field of scientific research, OTAVA-BB 1325766 is used as a subject for further investigation to understand its pharmacological properties and potential applications. This research can lead to the discovery of new therapeutic agents or contribute to the advancement of existing treatments.
Used in Chemical Synthesis:
OTAVA-BB 1325766 may also be utilized in chemical synthesis processes, where its unique structure can be employed to create new compounds with specific functions or properties. This application can be relevant across various industries, including pharmaceuticals, materials science, and environmental technology.

InChI:InChI=1/C13H9ClN2/c14-10-5-3-4-9(8-10)13-15-11-6-1-2-7-12(11)16-13/h1-8H,(H,15,16)

Upstream product

• 95-54-5 1,2-diamino-benzene 
• 535-80-8 3-chlorobenzoate 
• 587-04-2 m-Chlorobenzaldehyde 
• 88-74-4 2-nitro-aniline 
• 618-46-2 m-Chlorobenzoyl chloride 
• 1042161-49-8 C₁₃H₉ClN₄ 
• 51-17-2 benzoimidazole 
• 108-42-9 3-chloro-aniline 
• 766-80-3 1-bromomethyl-3-chlorobenzene 
• 873-63-2 m-chlorobenzyl alcohol 
• 62-53-3 aniline 
• 4152-90-3 m-chlorobenzylamine 
• 615-43-0 2-iodophenylamine 
• 108-41-8 1-chloro-3-methylbenzene 

Downstream Products

• 1148018-28-3 C₁₉H₁₂ClN₃O 
• 1081111-14-9 2-(3-chlorophenyl)-1-{3-[4-(3-acetylaminophenyl)piperidin-1-yl]propyl}-1H-benzimidazole 
• 1417819-12-5 2-chloro-6-phenylbenzo[4,5]imidazo[2,1-a]isoquinoline 
• 1417819-14-7 4-chloro-6-phenylbenzo[4,5]imidazo[2,1-a]isoquinoline 
• 1447946-61-3 C₂₇H₁₇ClN₂ 
• 1447946-62-4 C₂₇H₁₇ClN₂ 
• 1609007-45-5 (E)-1-(2-(3-chlorophenyl)-1H-benzo[d]imidazol-1-yl)-3-phenylprop-2-en-1-one 

Relevant articles and documents

Synthesis of 2-substituted benzimidazoles in the presence of polyaniline nanoparticles doped with 12-tungstophosphoric acid as reusable heterogeneous catalyst

Polyaniline nanoparticles doped with 12-tungstophosphoric acid was prepared with different loading amounts of 12-tungstophosphoric acid. Doped polyaniline was characterized by XRD, SEM, and FT-IR techniques and the Keggin anion of heteropoly acid was dete

Visible-Light Photoredox Catalyzed Double C-H Functionalization: Radical Cascade Cyclization of Ethers with Benzimidazole-Based Cyanamides

A visible-light photoredox catalyzed radical cascade cyclization of simple ethers with cyanamides is developed at room temperature. This strategy involves sequential inert Csp3-H/Csp2-H functionalizations through intermolecular addition reaction of oxyalkyl radicals to N-cyano groups followed by radical cyclization of iminyl radicals in situ generated with C-2 aryl rings. This method allows for efficient synthesis of tetracyclic benzo[4,5]imidazo[1,2-c]quinazolines. Importantly, this is the first example of an intermolecular-intramolecular radical cascade cyclization reaction of cyanamides.

Solvent-dependent metal-free chemoselective synthesis of benzimidazoles and 1,3,5-triarylbenzenes from 2-amino anilines and aryl alkyl ketones catalyzed by I2

A solvent-dependent I2-catalyzed chemoselective reaction was developed for the synthesis of benzimidazoles and 1,3,5-triarylbenzenes via the annulation of 2-amino anilines and aryl alkyl ketones or the cyclization of aryl alkyl ketones, respectively. With 1,4-dioxane as the solvent, sequential C[sbnd]N bond formation followed by C(CO)-C(CH3) bond cleavage leads to the formation of benzimidazoles in a highly selective manner while aldol-type self-condensation of aryl alkyl ketones predominates using PhNO2 or PhCl as the solvent to afford 1,3,5-triarylbenzenes.