41421-28-7

Basic information

• Product Name: 5-(3-CHLOROPHENYL)-1H-TETRAZOLE
• Synonyms: SALOR-INT L307882-1EA;5-(3-CHLOROPHENYL)TETRAZOLE;5-(3-CHLOROPHENYL)-1H-TETRAZOLE, 98+%;5-(m-Chlorophenyl)-1H-tetrazole;BUTTPARK 100\02-71;5-(3-CHLOROPHENYL)-1H-TETRAZOLE;5-(3-CHLORO-PHENYL)-2H-TETRAZOLE
• CAS NO: 41421-28-7
• Molecular Formula: C₇H₅ClN₄
• Molecular Weight: 180.59
• Mol File: 41421-28-7.mol
• Article Data: 64

Chemical Properties

• Melting Point: 139-140°C
• Boiling Point: 372.8°Cat760mmHg
• Flash Point: 211°C
• Appearance: /
• Density: 1.448g/cm³
• Vapor Pressure: 9.35E-06mmHg at 25°C
• BRN: 140081
• CAS DataBase Reference: 5-(3-CHLOROPHENYL)-1H-TETRAZOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(3-CHLOROPHENYL)-1H-TETRAZOLE(41421-28-7)
• EPA Substance Registry System: 5-(3-CHLOROPHENYL)-1H-TETRAZOLE(41421-28-7)

Safety Data

• Hazard Codes: Xn
• Statements: 22
• Safety Statements: S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.; S36:Wear suitable prot
• Hazardous Substances Data: 41421-28-7(Hazardous Substances Data)

Usage

General Description

5-(3-chlorophenyl)-1H-tetrazole is a chemical compound with the molecular formula C7H5ClN4. It is a tetrazole derivative, which is a class of heterocyclic compounds with a five-membered ring containing four nitrogen atoms. This particular compound has a chlorophenyl group attached to the tetrazole ring, which gives it unique chemical and physical properties. It is known for its use in pharmaceutical research and in the synthesis of other organic compounds. The compound has potential applications in the development of drugs, agrochemicals, and materials science. Its precise role and applications are still being explored in various fields of chemistry and related disciplines.

InChI:InChI=1/C7H4ClN4/c8-6-3-1-2-5(4-6)7-9-11-12-10-7/h1-4H/q-1

Upstream product

• 766-84-7 3-chloro-benzonitrile 
• 618-48-4 3-chlorobenzamide 
• 625-99-0 3-iodochlorobenzene 
• 587-04-2 m-Chlorobenzaldehyde 
• 108-37-2 1-bromo-3-chlorobenzene 
• 34158-71-9 3-chlorobenzaldehyde oxime 

Downstream Products

• 41420-93-3 2-(3-chlorophenyl)-5-methyl-1,3,4-oxadiazole 
• 79442-06-1 phenyl-2 (chloro-3 phenyl)-5 oxadiazole-1,3,4 
• 91658-57-0 [5-(3-Chloro-phenyl)-tetrazol-1-yl]-phenyl-methanone 
• 91658-62-7 [5-(3-Chloro-phenyl)-tetrazol-2-yl]-phenyl-methanone 
• 90278-24-3 5-(3-chloro-phenyl)-1-methyl-1H-tetrazole 
• 90278-25-4 5-(3′-chlorophenyl)-2-methyltetrazole 
• 92712-20-4 2-(1'-iodopropyn-3'-yl)-5-(m-chlorophenyl)tetrazole 
• 863713-21-7 2-(3-{[tert-butyl(dimethyl)silyl]oxy}-1-methylpropyl)-5-(3-chlorophenyl)-2H-tetrazole 
• 1077627-05-4 ethyl (Z)-3-[5-(3-chlorophenyl)-1H-tetrazol-1-yl]propenoate 
• 1077626-97-1 ethyl (E)-3-[5-(3-chlorophenyl)-1H-tetrazol-1-yl]propenoate 

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.]

Copper and nickel immobilized on cytosine@MCM-41: as highly efficient, reusable and organic–inorganic hybrid nanocatalysts for the homoselective synthesis of tetrazoles and pyranopyrazoles

In this work, a green approach is reported for efficient synthesis of biologically active tetrazole and pyranopyrazole derivatives in the presence of Cu-Cytosine@MCM-41 and Ni-Cytosine@MCM-41 (copper (II) and nickel (II) catalyst on the modified MCM-41 us