50907-23-8

Basic information

• Product Name: 5-(4-BROMO-PHENYL)-2H-TETRAZOLE
• Synonyms: BUTTPARK 49\01-68;5-(4-BROMO-PHENYL)-2H-TETRAZOLE;5-(4-BROMOPHENYL)-1H-TETRAZOLE;5-(4-BROMOPHENYL) TETRAZOLE;5-(p-Bromophenyl)-1H-tetrazole;5-(p-Bromophenyl)tetrazole;5-Bromo-2-(tetrazol-5-yl)benzene;1H-Tetrazole, 5-(4-broMophenyl)-
• CAS NO: 50907-23-8
• Molecular Formula: C₇H₅BrN₄
• Molecular Weight: 225.05
• EINECS: -0
• Product Categories: Building Blocks;Halogenated Heterocycles;Heterocyclic Building Blocks;Tetrazoles;TetrazolesHeterocyclic Building Blocks
• Mol File: 50907-23-8.mol
• Article Data: 119

Chemical Properties

• Melting Point: 260 °C (dec.)(lit.)
• Boiling Point: 374.6 °C at 760 mmHg
• Flash Point: 180.3 °C
• Appearance: /
• Density: 1.745
• Vapor Pressure: 8.27E-06mmHg at 25°C
• Storage Temp.: Room temperature.
• PKA: 3.95±0.10(Predicted)
• BRN: 141235
• CAS DataBase Reference: 5-(4-BROMO-PHENYL)-2H-TETRAZOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(4-BROMO-PHENYL)-2H-TETRAZOLE(50907-23-8)
• EPA Substance Registry System: 5-(4-BROMO-PHENYL)-2H-TETRAZOLE(50907-23-8)

Safety Data

• Hazard Codes: Xn
• Statements: 22-41
• Safety Statements: 26-39
• WGK Germany: 3
• Hazardous Substances Data: 50907-23-8(Hazardous Substances Data)

Usage

General Description

5-(4-Bromo-phenyl)-2H-tetrazole is a chemical compound with the molecular formula C7H5BrN4. It is a tetrazole derivative with a bromine atom attached to a phenyl group. Tetrazoles are a class of compounds known for their diverse biological activities, including antimicrobial, antiviral, and antitumor properties. 5-(4-Bromo-phenyl)-2H-tetrazole may have potential applications in the pharmaceutical and agrochemical industries due to its unique structure and potential biological activities. It is important to handle this chemical with care and follow proper safety protocols when working with it in the laboratory.

InChI:InChI=1/C7H4BrN4/c8-6-3-1-5(2-4-6)7-9-11-12-10-7/h1-4H/q-1

Upstream product

• 1122-91-4 4-bromo-benzaldehyde 
• 623-00-7 4-bromobenzenecarbonitrile 
• 5467-74-3 4-Bromophenylboronic acid 
• 67-68-5 dimethyl sulfoxide 
• 4648-54-8 trimethylsilylazide 
• 25062-46-8 4-bromobenzaldehyde oxime 
• 18039-42-4 5-Phenyl-1H-tetrazole 
• 207301-17-5 1-(4-bromophenyl)-4-ferrocenylmethylenetetrazolium fluoroborate 

Downstream Products

• 104186-20-1 4-[5-(4-Bromo-phenyl)-tetrazol-1-ylmethyl]-2,6-dimethyl-phenol 
• 21510-43-0 2-(4-bromophenyl)-5-phenyl-1,3,4-oxadiazole 
• 91658-56-9 1-benzoyl-5-(p-bromophenyl)tetrazole 
• 91658-61-6 2-benzoyl-5-(p-bromophenyl)tetrazole 
• 69746-31-2 5-(4-bromophenyl)-1-methyl-1H-tetrazole 
• 69746-36-7 5-(4-bromophenyl)-2-methyl-2H-tetrazole 
• 117594-25-9 N-[1-[5-(4-Bromo-phenyl)-tetrazol-1-yl]-1-phenyl-meth-(Z)-ylidene]-N'-(4-nitro-phenyl)-hydrazine 
• 117594-36-2 N-[1-[5-(4-Bromo-phenyl)-tetrazol-2-yl]-1-phenyl-meth-(Z)-ylidene]-N'-(4-nitro-phenyl)-hydrazine 
• 220843-12-9 2-(4-bromophenyl)-5-(4-(tert-butyl)phenyl)-1,3,4-oxadiazole 

Relevant articles and documents

The role of ruthenium and rhenium diimine complexes in conjugated polymers that exhibit interesting opto-electronic properties

This paper reports the synthesis and opto-electronic properties of different conjugated polymers that contain the diimine complexes of ruthenium or rhenium. Conjugated poly(phenylene vinylene)s that contain aromatic 1,3,4-oxadiazole and 2,2′-bipyridine un

Synthesis and characterization of magnetic Fe3O4@Creatinine@Zr nanoparticles as novel catalyst for the synthesis of 5-substituted 1H-tetrazoles in water and the selective oxidation of sulfides with classical and ultrasonic methods

Tetrazoles and sulfoxide compounds have a wide range of applications in industries and are of great expectation to be environmentally friendly and cost-effective. This paper reports the introduction of zirconium supported on Fe3O4 na

Practical scale up synthesis of carboxylic acids and their bioisosteres 5-substituted-1H-tetrazoles catalyzed by a graphene oxide-based solid acid carbocatalyst

Herein, catalytic application of a metal-free sulfonic acid functionalized reduced graphene oxide (SA-rGO) material is reported for the synthesis of both carboxylic acids and their bioisosteres, 5-substituted-1H-tetrazoles. SA-rGO as a catalytic material incorporates the intriguing properties of graphene oxide material with additional benefits of highly acidic sites due to sulfonic acid groups. The oxidation of aldehydes to carboxylic acids could be efficiently achieved using H2O2as a green oxidant with high TOF values (9.06-9.89 h?1). The 5-substituted-1H-tetrazoles could also be effectively synthesized with high TOF values (12.08-16.96 h?1). The synthesis of 5-substituted-1H-tetrazoles was corroborated by single crystal X-ray analysis and computational calculations of the proposed reaction mechanism which correlated well with experimental findings. Both of the reactions could be performed efficiently at gram scale (10 g) using the SA-rGO catalyst. SA-rGO displays eminent reusability up to eight runs without significant decrease in its productivity. Thus, these features make SA-rGO riveting from an industrial perspective.