127275-33-6

Basic information

• Product Name: 2-(4-Chloro-phenyl)-4,5-dimethyl-3,6-dihydro-2H-selenopyran
• Synonyms: 2-(4-Chloro-phenyl)-4,5-dimethyl-3,6-dihydro-2H-selenopyran
• CAS NO: 127275-33-6
• Molecular Weight: 285.675
• Mol File: 127275-33-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-(4-Chloro-phenyl)-4,5-dimethyl-3,6-dihydro-2H-selenopyran(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-Chloro-phenyl)-4,5-dimethyl-3,6-dihydro-2H-selenopyran(127275-33-6)
• EPA Substance Registry System: 2-(4-Chloro-phenyl)-4,5-dimethyl-3,6-dihydro-2H-selenopyran(127275-33-6)

Safety Data

• Hazardous Substances Data: 127275-33-6(Hazardous Substances Data)

Upstream product

• 62037-06-3 1-chloro-4-(dibromomethyl)benzene 
• 854278-31-2 dimethyl-selenocarbamic acid Se-[(4-chloro-phenyl)-dimethylcarbamoylselanyl-methyl] ester 
• 513-81-5 2,3-dimethyl-buta-1,3-diene 
• 104-88-1 4-chlorobenzaldehyde 
• 127275-30-3 2,4,6-Tris-(4-chloro-phenyl)-[1,3,5]triselenane 

Relevant articles and documents

Stannic chloride-induced unsymmetrical C-se bond cleavage of bis(N,N-dimethylcarbamoylseleno)methanes: Novel generation of selenoaldehydes

Treatment of bis(N,N-dimethylcarbamoylseleno)methanes with SnCl4 afforded β-1,3,5-triselenanes in moderate to high yields, and the key intermediates of the reactions, i.e., acylselonium ions and selenoaldehydes, were successfully trapped by usi

Efficient Synthesis of Selenocarbonyl Compounds by Treating Carbonyl Compounds with Bis(1,5-cyclooctanediylboryl) Selenide

Selenoaldehydes and selenoketones were generated in situ, by treating aldehydes or ketones, respectively, with bis(1,5-cyclooctanediylboryl) selenide; the resulting selenocarbonyl compounds were trapped with 2,3-dimethyl-1,3-butadiene to give the correspo