54196-61-1

Basic information

• Product Name: 2'',5-DICHLOOR-2-(3-METHYL-4H-1,2,4-TRIAZOOL-4-YL)BENZOFENON
• Synonyms: 2'',5-DICHLOOR-2-(3-METHYL-4H-1,2,4-TRIAZOOL-4-YL)BENZOFENON
• CAS NO: 54196-61-1
• Molecular Formula: C₁₆H₁₁Cl₂N₃O
• Molecular Weight: 332.18404
• Mol File: 54196-61-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 555.5°C at 760 mmHg
• Flash Point: 289.8°C
• Appearance: /
• Density: 1.38g/cm³
• Vapor Pressure: 2.22E-12mmHg at 25°C
• Refractive Index: 1.66
• CAS DataBase Reference: 2'',5-DICHLOOR-2-(3-METHYL-4H-1,2,4-TRIAZOOL-4-YL)BENZOFENON(CAS DataBase Reference)
• NIST Chemistry Reference: 2'',5-DICHLOOR-2-(3-METHYL-4H-1,2,4-TRIAZOOL-4-YL)BENZOFENON(54196-61-1)
• EPA Substance Registry System: 2'',5-DICHLOOR-2-(3-METHYL-4H-1,2,4-TRIAZOOL-4-YL)BENZOFENON(54196-61-1)

Safety Data

• Hazardous Substances Data: 54196-61-1(Hazardous Substances Data)

Usage

General Description

2'',5-DICHLOOR-2-(3-METHYL-4H-1,2,4-TRIAZOOL-4-YL)BENZOFENON is a chemical compound that contains two chlorine atoms, a benzophenone moiety, and a 4H-1,2,4-triazole ring with a methyl group. It is used in various industries, including pharmaceuticals, agriculture, and cosmetics. 2'',5-DICHLOOR-2-(3-METHYL-4H-1,2,4-TRIAZOOL-4-YL)BENZOFENON is commonly used as a UV filter in sunscreen and other personal care products due to its ability to absorb and block harmful UV radiation. Additionally, it is utilized as a photosensitizer in photodynamic therapy for cancer treatment and as a stabilizer in plastics and rubber products. However, it is important to handle this chemical with care, as prolonged exposure or ingestion can lead to harmful effects on human health and the environment.

InChI:InChI=1/C16H11Cl2N3O/c1-10-20-19-9-21(10)15-7-6-11(17)8-13(15)16(22)12-4-2-3-5-14(12)18/h2-9H,1H3

Upstream product

• 2958-36-3 (2-amino-5-chloro-phenyl)-(2-chloro-phenyl)-methanone 
• 64-18-6 formic acid 
• 54567-12-3 3-Amino-6-chloro-4-(2-chlorophenyl)-3,4-dihydro-4-hydroxy-2-methylquinazoline 

Relevant articles and documents

Novel synthesis of the pharmacologically important 1-substituted-6-phenyl-4H-s-triazolo[4,3-α][1,4]benzodiazepines

Several 6-phenyl-4H-s-triazolo[4,3-α][1,4]benzodiazepines have useful biological activity both in experimental animals and in man. This manuscript describes a novel synthesis of these compounds from intermediates that do not have a pre-formed benzodiazepine ring system.

Triazolyl benzophenone compounds

Intermediates of the formula IV: STR1 wherein R is selected from the group consisting of hydrogen and alkyl of 1 to 3 carbon atoms, inclusive; and wherein R2, R3, and R4 are selected from the group consisting of hydrogen, fluoro, chloro, bromo, nitro, and trifluoromethyl are produced by a multistep synthesis. The final compounds are tranquilizers and sedatives and can be used in mammals, including man, and in birds.