83442-19-7

Basic information

• Product Name: chloromethyl phenylselenide
• Synonyms: chloromethyl phenylselenide
• CAS NO: 83442-19-7
• Molecular Weight: 205.546
• Mol File: 83442-19-7.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: chloromethyl phenylselenide(CAS DataBase Reference)
• NIST Chemistry Reference: chloromethyl phenylselenide(83442-19-7)
• EPA Substance Registry System: chloromethyl phenylselenide(83442-19-7)

Safety Data

• Hazardous Substances Data: 83442-19-7(Hazardous Substances Data)

Upstream product

• 593-71-5 Chloroiodomethane 
• 1666-13-3 diphenyl diselenide 
• 23974-72-3 sodium phenylselenide 
• 22859-16-1 tris(phenylselanyl)methane 
• 75-09-2 dichloromethane 

Downstream Products

• 127956-02-9 ethyl 1-benzyl-4-oxo-3-phenylselenomethyl-3-piperidinecarboxylate 
• 127956-00-7 ethyl 1-benzyl-3-oxo-4-phenylselenomethyl-4-piperidinecarboxylate 
• 335164-91-5 2-[(phenylseleno)methoxy]benzaldehyde 
• 61759-13-5 1-(phenylselanyl)propan-2-one 
• 28897-11-2 2-methyl-1-(phenylselanyl)propan-2-ol 
• 861391-83-5 phenylselenomethyl (E)-(2RS)-2-benzyl-4-(4-methoxyphenyl)-3-butenoate 
• 1027917-83-4 5-chloro-2-phenylselanylmethoxy-phenylamine 
• 732299-20-6 (5-chloro-2-phenylselanylmethoxy-phenyl)-(2-phenyl-propenylidene)-amine 
• 732299-14-8 diphenylvinylidene-(2-phenylselanylmethoxy-phenyl)-amine 
• 732299-15-9 diphenylvinylidene-(5-methyl-2-phenylselanylmethoxy-phenyl)-amine 
• 732299-19-3 (5-chloro-2-phenylselanylmethoxy-phenyl)-diphenylvinylidene-amine 
• 732299-18-2 diphenylvinylidene-(4-methyl-2-phenylselanylmethoxy-phenyl)-amine 
• 732299-16-0 diphenylvinylidene-(5-methoxy-2-phenylselanylmethoxy-phenyl)-amine 

Relevant articles and documents

Preparation method of antiviral phenyl selenide

The invention discloses a preparation method of an antiviral phenyl selenide. The method comprises the following steps: under nitrogen protection, by taking sodium borohydride as a reducing agent, reacting diphenyl diselenide with dichloromethane to synth

Synthesis and antitumor activity of selenium-containing quinone-based triazoles possessing two redox centres, and their mechanistic insights

Selenium-containing quinone-based 1,2,3-triazoles were synthesized using click chemistry, the copper catalyzed azide-alkyne 1,3-dipolar cycloaddition, and evaluated against six types of cancer cell lines: HL-60 (human promyelocytic leukemia cells), HCT-11

Imidazolium ionic liquids containing selenium: Synthesis and antimicrobial activity

The synthesis and antimicrobial profile of imidazolium ionic liquids containing selenium are described herein. Minimum inhibitory concentration revealed that these compounds are especially active against algae, and their activity is modulated by substitue