14832-59-8

Basic information

• Product Name: N-(5H-tetrazol-5-ylidene)aniline
• CAS NO: 14832-59-8
• Molecular Formula: C₇H₇N₅
• Molecular Weight: 159.1481
• Mol File: 14832-59-8.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 228.2°C at 760 mmHg
• Flash Point: 83.3°C
• Density: 1.42g/cm³
• Vapor Pressure: 0.112mmHg at 25°C
• Refractive Index: 1.738
• CAS DataBase Reference: N-(5H-tetrazol-5-ylidene)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: N-(5H-tetrazol-5-ylidene)aniline(14832-59-8)
• EPA Substance Registry System: N-(5H-tetrazol-5-ylidene)aniline(14832-59-8)

Safety Data

• Hazardous Substances Data: 14832-59-8(Hazardous Substances Data)

Upstream product

• 622-34-4 1-phenylcyanamide 
• 103-72-0 phenyl isothiocyanate 
• 103-85-5 monophenylthiourea 
• 591-50-4 iodobenzene 
• 88104-34-1 1-benzyl-N-phenyl-1H-tetrazol-5-amine 
• 108-90-7 chlorobenzene 
• 108-86-1 bromobenzene 
• 4921-82-8 1-benzoyl-3-phenylthiourea 
• 5467-78-7 fenamole 
• 107-21-1 ethylene glycol 

Downstream Products

• 99359-10-1 N-(1-phenyl-1H-tetrazol-5-yl)-acetamide 
• 5467-78-7 fenamole 
• 1197040-29-1 phenyl isocyanate 
• 114065-68-8 [5-tert-Butyl-2-(2,4-dinitro-phenyl)-2H-[1,2,4]triazol-3-yl]-phenyl-amine 
• 114065-77-9 [5-tert-Butyl-2-(4-nitro-phenyl)-2H-[1,2,4]triazol-3-yl]-phenyl-amine 
• 164333-97-5 (2-dodecyl-2H-tetrazol-5-yl)phenylamine 
• 864814-33-5 [2-(10-Methyl-undecyl)-2H-tetrazol-5-yl]-phenyl-amine 
• 864814-11-9 Phenyl-(2-tetradecyl-2H-tetrazol-5-yl)-amine 
• 864814-10-8 (2-Pentyl-2H-tetrazol-5-yl)-phenyl-amine 

Relevant articles and documents

Iron-mediated desulphurization approach: synthesis of cyanamides and their conversions

The iron-mediated efficient multi-component method has been demonstrated for the synthesis of substituted cyanamides from isothiocyanates under mild reaction conditions. Subsequent nucleophilic addition and desulfurization are involved in this proposed synthetic methodology. All the reactions are rapid, facile, and accomplished at room temperature. A variety of substrates readily underwent the optimized reaction conditions to provide their respective target products in good to excellent yields. Furthermore, we have confirmed that no other by-products could be identified during our experimental reaction process. Graphical abstract: Iron-mediated efficient multi-component method has been demonstrated for the synthesis of substituted cyanamides from isothiocyanates under mild reaction conditions. Subsequent nucleophilic addition and desulfurization are involved in this proposed synthetic methodology.[Figure not available: see fulltext.].

Palladium-catalyzed N-Arylation of 1-substituted-1H-tetrazol-5-amines

A palladium-catalyzed N-arylation of 1-substituted-1H-tetrazol-5-amines has been described for the first time. The reaction provides good yields of desired products with broad substrate scope and good functional group tolerance.

CoFe2O4 nanoparticles as a magnetically recoverable and reusable catalyst for the synthesis of arylaminotetrazoles and 5-aryloxytetrazoles

An efficient and direct method is described for the synthesis of 5-arylamino-1H-tetrazoles (Isomer A) or 1-aryl-5-amino-1Htetrazoles (Isomer B) and 5-aryloxytetrazoles from arylcyanamides or cynates with nano CoFe 2O4 as a reusable a