4426-68-0

Basic information

• Product Name: Benzene, isoselenocyanato-
• Synonyms: Benzene, isoselenocyanato-
• CAS NO: 4426-68-0
• Molecular Formula: C₇H₅NSe
• Molecular Weight: 182.08
• Mol File: 4426-68-0.mol
• Article Data: 37

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzene, isoselenocyanato-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, isoselenocyanato-(4426-68-0)
• EPA Substance Registry System: Benzene, isoselenocyanato-(4426-68-0)

Safety Data

• Hazardous Substances Data: 4426-68-0(Hazardous Substances Data)

Upstream product

• 1197040-29-1 phenyl isocyanate 
• 622-44-6 phenylcarbonimidic dichloride 
• 506-80-9 carbon diselenide 
• 62-53-3 aniline 
• 103-71-9 phenyl isocyanate 
• 103-70-8 Formanilid 
• 75-44-5 phosgene 
• 698-16-8 benzohydroximoyl chloride 
• 245539-09-7 2,3-dichlorophenyl isocyanide 
• 7782-49-2 selenium 
• 67-66-3 chloroform 
• 64-18-6 formic acid 

Downstream Products

• 16519-43-0 1,3-diphenyl-selenourea 
• 854887-59-5 N-[2]naphthyl-N'-phenyl-selenourea 
• 6124-05-6 1-methyl-3-phenyl-selenourea 
• 6124-02-3 N-phenylselenourea 
• 14223-50-8 N-phenylhydrazinecarboselenoamide 
• 16519-53-2 N-(4-methoxyphenyl)-N'-phenylselenourea 
• 14223-83-7 1,4-diphenylselenosemicarbazide 
• 67766-77-2 phenyl-(3,4,4-trimethyl-5-methylene-selenazolidin-2-ylidene)-amine 
• 67972-01-4 (4-ethyl-4-methyl-5-methylene-4,5-dihydro-selenazol-2-yl)-phenyl-amine 
• 67766-78-3 (4-ethyl-3,4-dimethyl-5-methylene-selenazolidin-2-ylidene)-phenyl-amine 
• 40700-13-8 3-phenyl-4,5,6,7-tetrahydro-3H-benzothiazole-2-selone 
• 40700-11-6 3-phenyl-3H-thiazole-2-selone 
• 67972-02-5 (4-methyl-5-methylene-4-propyl-4,5-dihydro-selenazol-2-yl)-phenyl-amine 
• 16519-50-9 N-Phenyl-N'-o-tolyl-selenoharnstoff 

Relevant articles and documents

A facile preparation of selenohydantoins using isoselenocyanate

(Chemical Equation Presented) Reactions of isoselenocyanate with methyl aminoacetate hydrochlorides in the presence of triethylamine afforded selenohydantoins, 2-selenoxoimidazolidin-4-ones, in high yields.

Room-Temperature Metal-Free Multicomponent Polymerizations of Elemental Selenium toward Stable Alicyclic Poly(oxaselenolane)s with High Refractive Index

Selenium-containing polymers are a group of fascinating functional polymers with unique structures, properties, and applications, which have been developed recently but only with limited examples. The challenges of developing selenium-containing polymers

Bis-Selenoureas for Anion Binding: A 1H NMR and Theoretical Study

The anion binding ability of a family of bis-selenoureas L1-L3 obtained by the reaction of 1,3-bis(aminomethyl)-benzene and phenylisoselenocyanate, p-methoxyphenylisoselenocyanate and naphtylisoselenocyanate, for L1, L2, and L3, respectively, has been tested and compared to that of previously described bis-urea analogues. Results suggest that the introduction of selenium leads to an increase in the acidity of the urea NH hydrogen atoms, and therefore to a stronger affinity (more than three-fold higher) towards anion species, in particular dihydrogen phosphate, in DMSO-d6. Theoretical calculations allowed for the optimization of the adducts receptors corroborating the experimental results.