126393-38-2

Basic information

• Product Name: 5-[4-(TERT-BUTYL)PHENYL]-2H-1,2,3,4-TETRAAZOLE
• Synonyms: BUTTPARK 50\02-66;5-[4-(TERT-BUTYL)PHENYL]-2H-1,2,3,4-TETRAAZOLE;5-(4-TERT-BUTYLPHENYL)TETRAZOLE;5-[4-(tert-Butyl)phenyl]-2H-1,2,3,4-tetrazole, 97%;5-(4-(tert-Butyl)phenyl)-2H-tetrazole
• CAS NO: 126393-38-2
• Molecular Formula: C₁₁H₁₄N₄
• Molecular Weight: 202.26
• Mol File: 126393-38-2.mol
• Article Data: 3

Chemical Properties

• Melting Point: 193-195
• Boiling Point: 344.5°Cat760mmHg
• Flash Point: 152.9°C
• Appearance: /
• Density: 1.127g/cm³
• Vapor Pressure: 6.57E-05mmHg at 25°C
• Refractive Index: 1.559
• PKA: 4.43±0.10(Predicted)
• CAS DataBase Reference: 5-[4-(TERT-BUTYL)PHENYL]-2H-1,2,3,4-TETRAAZOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-[4-(TERT-BUTYL)PHENYL]-2H-1,2,3,4-TETRAAZOLE(126393-38-2)
• EPA Substance Registry System: 5-[4-(TERT-BUTYL)PHENYL]-2H-1,2,3,4-TETRAAZOLE(126393-38-2)

Safety Data

• Hazard Codes: F
• Statements: R11:Highly flammable.
• Safety Statements: S16:Keep away from sources of ignition - No smoking.
• Hazardous Substances Data: 126393-38-2(Hazardous Substances Data)

Usage

General Description

. 5-[4-(tert-butyl)phenyl]-2H-1,2,3,4-tetraazole is a chemical compound with the molecular formula C13H16N4. It is a tetraazolyl derivative with a tert-butylphenyl group. 5-[4-(TERT-BUTYL)PHENYL]-2H-1,2,3,4-TETRAAZOLE is used in the field of organic chemistry and pharmaceutical research for its potential biological activities. It has been studied for its potential as an antihypertensive agent and has also shown potential in the treatment of central nervous system disorders. Moreover, it has been investigated for its role as a vasodilator and potential use in the treatment of erectile dysfunction. Its unique chemical structure and potential pharmacological properties make it an interesting compound for further research and development.

InChI:InChI=1/C11H14N4/c1-11(2,3)9-6-4-8(5-7-9)10-12-14-15-13-10/h4-7H,1-3H3,(H,12,13,14,15)

Upstream product

• 4210-32-6 4-tert-butyl benzonitrile 
• 67-68-5 dimethyl sulfoxide 
• 123324-71-0 p-tert-butylphenylboronic acid 
• 636-70-4 triethylamine hydrobromide 
• 3972-65-4 1-bromo-4-tert-butylbenzene 

Downstream Products

• 876173-84-1 2-bromo-2'-(4-tert-butylphenyl-1H-tetrazol-5-yl)-9,9'-spirobifluorene 
• 876173-85-2 2,7-dibromo-2'-(4-tert-butylphenyl-1H-tetrazol-5-yl)-9,9'-spirobifluorene 
• 1380108-85-9 2-(6-(7-(9H-carbazol-9-yl)-9,9-dihexyl-9H-fluoren-2-yl)pyridin-3-yl)-5-(4-tert-butylphenyl)-1,3,4-oxadiazole 
• 1380108-91-7 2-(4-tert-butylphenyl)-5-(6-chloropyridin-3-yl)-1,3,4-oxadiazole 
• 480390-99-6 methyl 2-[5-(4-t-butylphenyl)-1,3,4-oxadiazol-2-yl]benzoate 
• 480391-09-1 methyl 4-[5-(4-t-butylphenyl)-1,3,4-oxadiazol-2-yl]-3-nitrobenzoate 
• 1393600-92-4 C₅₄H₅₄N₄O₂ 
• 193614-95-8 3,5-bis[5-(4-tert-butylphenyl)-1,3,4-oxadiazol-2-yl]bromobenzene 
• 480390-92-9 methyl 4-(5-(4-(tbutyl)phenyl)-1,3,4-oxadiazol-2-yl)benzoate 

Relevant articles and documents

Conversion of Arylboronic Acids to Tetrazoles Catalyzed by ONO Pincer-Type Palladium Complex

A convenient synthesis of a library of tetrazoles through a novel and operationally simple protocol effecting the direct conversion of arylboronic acids catalyzed by a new ONO pincer-type Pd(II) complex under mild reaction conditions using the readily available reagents is reported. The palladium complex was reused up to four cycles in an open-flask condition.

USE OF SPIRO COMPOUNDS AS LASER DYES

Use of spiro compounds of formula (I), where K and K are, independently of one another, conjugated systems, as a laser dye.