2835-58-7

Basic information

• Product Name: 2-(phenylazo)aniline
• Synonyms: 2-(phenylazo)aniline;2-aminoazobenzene;Azobenzen-2-amine
• CAS NO: 2835-58-7
• Molecular Formula: C₁₂H₁₁N₃
• Molecular Weight: 197.23584
• EINECS: 220-610-2
• Mol File: 2835-58-7.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 362.4°Cat760mmHg
• Flash Point: 173°C
• Appearance: /
• Density: 1.12g/cm³
• Vapor Pressure: 1.94E-05mmHg at 25°C
• Refractive Index: 1.611
• CAS DataBase Reference: 2-(phenylazo)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(phenylazo)aniline(2835-58-7)
• EPA Substance Registry System: 2-(phenylazo)aniline(2835-58-7)

Safety Data

• Hazardous Substances Data: 2835-58-7(Hazardous Substances Data)

Usage

General Description

2-(phenylazo)aniline, also known as benzene diazonium-4-aminobenzene, is an organic compound with the molecular formula C12H10N2. It is a diazo compound that is commonly used in the production of azo dyes. It is a red-orange solid that is sparingly soluble in water but soluble in organic solvents. 2-(phenylazo)aniline is an azo compound, which means it contains a nitrogen-nitrogen double bond. It is also known for its use in the synthesis of pharmaceutical compounds and as a reagent in organic chemistry reactions. This chemical is a known skin and eye irritant and should be handled with care in a laboratory setting.

InChI:InChI=1/C12H11N3/c13-11-8-4-5-9-12(11)15-14-10-6-2-1-3-7-10/h1-9H,13H2/b15-14+

Upstream product

• 858784-43-7 1,2-bis-(N'-phenyl-hydrazino)-benzene 
• 15719-64-9 methylammonium carbonate 
• 98-95-3 nitrobenzene 
• 95-54-5 1,2-diamino-benzene 
• 603-11-2 3-nitrophthalic acid 
• 62-53-3 aniline 
• 622-37-7 Phenyl azide 
• 142-04-1 aniline hydrochloride 
• 297766-64-4 1,3-Diphenyltriazen 
• 721-47-1 2'-Aminobenzanilid 
• 17277-44-0 ortho-azidoazobenzene 
• 110-82-7 cyclohexane 
• 7310-83-0 2- benzoylaminoazobenzene 
• 146651-75-4 tert–butyl (2–aminophenyl)carbamate 

Downstream Products

• 17716-46-0 2-acetamidoazobenzene 
• 30672-26-5 2-(phenylazo)azobenzene 
• 313485-89-1 N-phenyl-1H-benzo[d]imidazol-1-amine 
• 1916-72-9 2-phenyl-2H-1,2,3-benzotriazole 
• 51750-18-6 2-phenyl-2H-benzotriazole 1-oxide 
• 62-53-3 aniline 
• 95-54-5 1,2-diamino-benzene 
• 53314-18-4 2-Amino-hydrazobenzol 
• 2362-57-4 2-phenylazo-phenol 
• 861783-88-2 1-anilino-2-phenylbenzimidazole 
• 5021-43-2 2-phenylquinoxaline 
• 643740-39-0 [AuCl₂(NHC₆H₄NNC₆H₅)] 
• 669700-81-6 [Pt(HNC₆H₄NNC₆H₅)2] 
• 863457-62-9 [(2-(phenylazo)aniline(-1H))(aniline)RhCl₂] 

Relevant articles and documents

A non-nucleoside triphosphate for powering kinesin-microtubule motility with photo-tunable velocity

Three non-nucleoside triphosphates, one containing an azobenzene moiety, power a kinesin-microtubule system with high motile activity, with an observed maximum velocity of almost half of that obtained with ATP. The cis-trans photoisomerization of the azobenzene unit allows reversible and repeated control over the motile properties of kinesin.

Cannabinoid receptor light-operated ligand and preparation method and application thereof

The invention relates to the technical field of biology, in particular to a novel cannabinoid receptor light-operated ligand and a preparation method and application thereof. Disclosed is the cannabinoid receptor light-operated ligand or the isomer prodrug, the solvate and the pharmaceutically acceptable salt of the cannabinoid receptor light-operated ligand, wherein the structural formula of thecannabinoid receptor light-operated ligand is A-linker-B; A is a transmembrane domain ligand structure, and B is a light-operated element; Linker is a subunit which is linear and has no activity on acannabinoid receptor light-operated ligand. According to the invention, the cannabinoid receptor ligand is integrated with azobenzene through a proper connector, so that the ligand configuration is changed under an illumination condition, and the activation or inhibition state of the cannabinoid receptor is regulated and controlled.

Palladium-catalyzed annulation of 2-(aryldiazenyl) aniline with dimethyl sulfoxide to access N-aryl-1H-benzo[d]imidazol-1-amine

A palladium-catalyzed annulation of 2-(aryldiazenyl) aniline and dimethyl sulfoxide was developed to access N-aryl-1H-benzo[d]imidazol-1-amine in moderate to good yields. Activated by 1,4-diazabicyclo[2.2.2]octane bis(sulfur dioxide) adduct (DABSO), DMSO served as a “[dbnd]CH[sbnd]” fragment during this procedure. It represents a facile pathway leading to benzimidazoles.