50907-46-5

Basic information

• Product Name: 5-(2-CHLOROPHENYL)-1H-TETRAZOLE
• Synonyms: 1H-TETRAZOLE, 5-(2-CHLOROPHENYL)-;5-(2-CHLOROPHENYL)-1H-1,2,3,4-TETRAAZOLE;5-(2-CHLOROPHENYL)-1H-TETRAZOLE;5-(2-Chlorophenyl)tetrazole;5-(2-Chloro-phenyl)-2H-tetrazole;5-(o-Chlorophenyl)-1H-tetrazole;5-(2-Chlorophenyl)-2h-1,2,3,4-tetrazole;5-(2-Chlorophenyl)-1H-tetrazole
• CAS NO: 50907-46-5
• Molecular Formula: C₇H₅ClN₄
• Molecular Weight: 180.59
• Mol File: 50907-46-5.mol
• Article Data: 92

Chemical Properties

• Melting Point: 179-180°C
• Boiling Point: 367.5°Cat760mmHg
• Flash Point: 207.6°C
• Appearance: /
• Density: 1.448g/cm³
• Vapor Pressure: 1.36E-05mmHg at 25°C
• Refractive Index: 1.631
• Solubility: soluble in Methanol
• PKA: 3.78±0.10(Predicted)
• BRN: 148559
• CAS DataBase Reference: 5-(2-CHLOROPHENYL)-1H-TETRAZOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(2-CHLOROPHENYL)-1H-TETRAZOLE(50907-46-5)
• EPA Substance Registry System: 5-(2-CHLOROPHENYL)-1H-TETRAZOLE(50907-46-5)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36
• Hazardous Substances Data: 50907-46-5(Hazardous Substances Data)

Usage

Uses

5-(2-CHLOROPHENYL)-1H-TETRAZOLE is a useful research chemical.

InChI:InChI=1/C7H5ClN4/c8-6-4-2-1-3-5(6)7-9-11-12-10-7/h1-4H,(H,9,10,11,12)

Upstream product

• 15717-17-6 2-chlorothiobenzamide 
• 17849-38-6 2-Chlorobenzyl alcohol 
• 873-32-5 2-Chlorobenzonitrile 
• 3717-28-0 2-chloro benzaldehyde oxime 
• 89-98-5 2-chloro-benzaldehyde 
• 74115-29-0 2-chloro-N'-(2-chloro-benzylidene)-benzohydrazonoyl chloride 
• 5328-80-3 2-chlorobenzaldehyde N-[(2-chlorophenyl)methylidene]hydrazone 
• 609-66-5 2-chlorobenzamide 
• 624-84-0 formic acid hydrazide 
• 709041-72-5 5-(2-chloro-phenyl)-tetrazol-1-ylamine 

Downstream Products

• 117594-28-2 N-[1-[5-(2-Chloro-phenyl)-tetrazol-1-yl]-1-phenyl-meth-(Z)-ylidene]-N'-(4-nitro-phenyl)-hydrazine 
• 117594-39-5 N-[1-[5-(2-Chloro-phenyl)-tetrazol-2-yl]-1-phenyl-meth-(Z)-ylidene]-N'-(4-nitro-phenyl)-hydrazine 
• 77455-52-8 5-(2-chlorophenyl)-1-methyl-1H-tetrazole 
• 77455-51-7 5-(2′-chlorophenyl)-2-methyltetrazole 
• 139111-38-9 (2-chlorobenz)amidrazone 
• 1077627-04-3 ethyl (Z)-3-[5-(2-chlorophenyl)-1H-tetrazol-1-yl]propenoate 
• 950231-30-8 2-(2-chlorolphenyl)-5-(5-methyl-1-phenyl-1H-1,2,3-triazol-4-yl)-1,3,4-oxadiazole 
• 1361119-80-3 1-(4-(5-(2-chlorophenyl)-2H-tetrazol-2-yl)phenyl)ethanone 
• 1361119-79-0 5-(2-chlorophenyl)-2-(4-methoxyphenyl)-2H-tetrazole 
• 117594-51-1 [3-(2-Chloro-phenyl)-5-phenyl-[1,2,4]triazol-4-yl]-(4-nitro-phenyl)-amine 
• 117594-48-6 5-(2-Chloro-phenyl)-1-(4-nitro-phenyl)-3-phenyl-1H-[1,2,4]triazole 
• 24023-72-1 2‐(chloromethyl)‐5‐(2‐chlorophenyl)‐1,3,4‐oxadiazole 

Relevant articles and documents

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

Synthesis and Characterization of Magnetic Functionalized Ni and Cu Nano Catalysts and Their Application in Oxidation, Oxidative Coupling and Various Multi-Component Reactions

Abstract: Two magnetic nano catalysts of nickel and copper, Fe3O4@SiO2@DOP-BenPyr-M(II), (M=Ni and Cu) have been synthesized. These catalysts were applied as recoverable, efficient and new heterogeneous catalysts for the high yielding and room temperature one-pot procedure of selective oxidation of sulfides to sulfoxides and oxidative coupling of thiols to disulfides. In addition, the catalytic activity of Fe3O4@SiO2@DOP-BenPyr-Ni(II) was investigated as heterogeneous nanocatalyst for synthesis of 2,3-dihydroquinazolin-4(1H)-ones, 5-substituted 1H-tetrazoles and polyhydroquinolines. The synthesized catalysts were characterized by FT-IR, TGA, XRD, VSM, EDX, ICP and SEM techniques. These catalysts were recovered by an external magnet and reused several times without significant loss of catalytic efficiency. Graphic Abstract: [Figure not available: see fulltext.]

Coupling ofN-tosylhydrazones with tetrazoles: synthesis of 2-β-d-glycopyranosylmethyl-5-substituted-2H-tetrazole type glycomimetics

Coupling reactions ofO-peracylated 2,6-anhydro-aldose tosylhydrazones (C-(β-d-glycopyranosyl)formaldehyde tosylhydrazones) with tetrazoles were studied under metal-free conditions using thermic or microwave activation in the presence of different bases. The reactions proved highly regioselective and gave the corresponding, up-to-now unknown 2-β-d-glycopyranosylmethyl-2H-tetrazoles in 7-67% yields. The method can be applied to get new types of disaccharide mimetics, 5-glycosyl-2-glycopyranosylmethyl-2H-tetrazoles, as well. Galectin binding studies withC-(β-d-galactopyranosyl)formaldehyde tosylhydrazone and 2-(β-d-galactopyranosylmethyl)-5-phenyl-2H-tetrazole revealed no significant inhibition of any of these lectins.