14210-51-6

Basic information

• Product Name: 2-(1H-TETRAZOL-1-YL)ANILINE
• Synonyms: AKOS BB-8756;2-(1H-TETRAZOL-1-YL)ANILINE;CHEMBRDG-BB 4002015;AKOS BBV-014094;UKRORGSYN-BB BBV-014094;2-(1H-tetrazol-1-yl)aniline(SALTDATA: FREE)
• CAS NO: 14210-51-6
• Molecular Formula: C₇H₇N₅
• Molecular Weight: 161.16
• Mol File: 14210-51-6.mol
• Article Data: 3

Chemical Properties

• Melting Point: 98-99 °C
• Boiling Point: 366.121°C at 760 mmHg
• Flash Point: 175.224°C
• Appearance: /
• Density: 1.467g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.749
• PKA: 1.26±0.10(Predicted)
• CAS DataBase Reference: 2-(1H-TETRAZOL-1-YL)ANILINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(1H-TETRAZOL-1-YL)ANILINE(14210-51-6)
• EPA Substance Registry System: 2-(1H-TETRAZOL-1-YL)ANILINE(14210-51-6)

Safety Data

• Hazardous Substances Data: 14210-51-6(Hazardous Substances Data)

Usage

General Description

2-(1H-Tetrazol-1-yl)aniline is a chemical compound with the molecular formula C7H7N5. It is an aromatic amine that contains a 1H-tetrazole group. 2-(1H-TETRAZOL-1-YL)ANILINE is used in the synthesis of pharmaceuticals and organic compounds due to its unique chemical properties. It is also used as a building block in the development of agrochemicals, dyes, and other fine chemicals. Additionally, 2-(1H-Tetrazol-1-yl)aniline has potential applications in the field of biochemistry and medicinal chemistry due to its ability to interact with biological molecules. Overall, this compound has broad utility and potential in various industrial and scientific applications.

InChI:InChI=1/C7H7N5/c8-6-3-1-2-4-7(6)12-5-9-10-11-12/h1-5H,8H2

Upstream product

• 88-74-4 2-nitro-aniline 
• 14210-50-5 1-(2-nitrophenyl)-1H-1,2,3,4-tetrazole 

Downstream Products

• 1356660-55-3 N-(2-(1H-tetrazol-1-yl)phenyl)-2,3-dichlorobenzenesulfonamide 
• 1063940-07-7 4-(4-bromo-phenyl)-tetrazolo[1,5-a]quinoxaline 
• 1063940-10-2 4-(2-hydroxyphenyl)-tetrazolo[1,5-a]quinoxaline 
• 1063940-08-8 4-(4-chloro-phenyl)-tetrazolo[1,5-a]quinoxaline 
• 406713-50-6 4-p-tolyl-tetrazolo[1,5-a]quinoxaline 
• 133638-20-7 1,1′-(1,2-phenylene)bis(1H-1,2,3,4-tetrazole) 

Relevant articles and documents

Synthesis of highly functionalized polycyclic quinoxaline derivatives using visible-light photoredox catalysis

A mild and facile method for preparing highly functionalized pyrrolo[1,2-a]quinoxalines and other nitrogenrich heterocycles, each containing a quinoxaline core or an analogue thereof, has been developed. The novel method features a visible-light-induced decarboxylative radical coupling of ortho-substituted arylisocyanides and radicals generated from phenyliodine(III) dicarboxylate reagents and exhibits excellent functional group compatibility. A wide range of quinoxaline heterocycles have been prepared. Finally, a telescoped preparation of these polycyclic compounds by integration of the in-line isocyanide formation and photochemical cyclization has been established in a three-step continuousflow system.

SYNTHESIS AND PROPERTIES OF PHENYLENEBIS-1H-TETRAZOLES

Heterocyclization of m- and p-phenylenediamines with orthoformic ester and sodium azide has given phenylenebis-1H-tetrazoles.Under these conditions, o-phenylenediamine gives benzimidazole. o-, m-, and p-Phenylenebis-1H-tetrazoles were also obtained from the nitroanilines via the intermediate nitro- and aminophenyltetrazoles.The reactions of the bistetrazoles examined were basic hydrolysis, aminomethylation, and complex formation with copper salts.