16519-43-0

Basic information

• Product Name: (diphenylcarbamimidoyl)selanyl
• CAS NO: 16519-43-0
• Molecular Formula: C₁₃H₁₂N₂Se
• Molecular Weight: 274.1998
• Mol File: 16519-43-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (diphenylcarbamimidoyl)selanyl(CAS DataBase Reference)
• NIST Chemistry Reference: (diphenylcarbamimidoyl)selanyl(16519-43-0)
• EPA Substance Registry System: (diphenylcarbamimidoyl)selanyl(16519-43-0)

Safety Data

• Hazardous Substances Data: 16519-43-0(Hazardous Substances Data)

Usage

General Description

"(Diphenylcarbamimidoyl)selanyl" is a chemical compound that consists of a selenium atom bonded to two phenyl groups and a carbamimidoyl group. It is commonly used in organic synthesis and has been studied for its potential biological and pharmaceutical applications. (diphenylcarbamimidoyl)selanyl has been found to exhibit antioxidant and anti-inflammatory properties, and it may also have some potential as an antitumor agent. Additionally, (diphenylcarbamimidoyl)selanyl has been investigated for its role in redox signaling and its ability to modulate cellular processes. It represents an area of ongoing research in the field of selenium chemistry and its implications for human health.

Upstream product

• 62-53-3 aniline 
• 4426-68-0 phenyl isoselenocyanate 
• 506-80-9 carbon diselenide 
• 931-53-3 Cyclohexyl isocyanide 
• 102-08-9 N,N-diphenylthiourea 
• 622-16-2 1,3-Diphenylcarbodiimide 
• 5416-30-8 N,N'-diphenyl-S-methyl isothiourea 
• 67-66-3 chloroform 
• 60006-92-0 S-methyl-N,N'-diphenyl-isothiourea; hydriodide 
• 1197040-29-1 phenyl isocyanate 

Downstream Products

• 64850-92-6 2-(9H-Fluoren-9-yl)-1,3-diphenyl-isoselenourea 
• 66497-26-5 4-oxo-3-phenyl-2-phenylimino-3,4-dihydro-2H-[1,3]selenazine-6-carboxylic acid methyl ester 
• 1241921-16-3 methyl 4-hydroxy-3-phenyl-5-(2-phenylethyl)-2-phenyl-iminoselenazolidine-4-carboxylate 
• 1241921-17-4 methyl 5-hexyl-4-hydroxy-3-phenyl-2-phenyliminoselenazolidine-4-carboxylate 
• 1241921-09-4 methyl 4-hydroxy-3,5-diphenyl-2-phenyliminoselenazolidine-4-carboxylate 
• 1241921-10-7 1-phenylimino-3-phenylselenazolo[3,4-a]quinoxalin-4(5H)-one 
• 1241921-18-5 1-phenylimino-3-(2-phenylethyl)selenazolo[3,4-a]quinoxalin-4(5H)-one 
• 1241921-11-8 7,8-dimethyl-1-phenylimino-3-(2-phenylethyl)selenazolo-[3,4-a]quinoxalin-4(5H)-one 
• 1241921-14-1 8-nitro-1-phenylimino-3-(2-phenylethyl)selenazolo[3,4-a]-quinoxalin-4(5H)-one 
• 39510-74-2 methyl α,χ-diphenylallophanate 
• 64287-36-1 phenyl-(1-phenyl-1H-tetrazol-5-yl)-amine 
• 681429-25-4 [Pt(SeC(NC₆H₅)NC₆H₅)(P(C₆H₅)3)2] 
• 603-54-3 N,N-diphenylurea 
• 101-01-9 N,N',N''-triphenylguanidine 

Relevant articles and documents

Efficient synthesis of selenoureas from the corresponding carbodiimides

Selenoureas were synthesized by the reaction of carbodiimides with LiA1HSeH in the presence of hydrogen chloride.

Selenoureas for anion binding as molecular logic gates

The first example of a molecular logic gate based on selenourea/anion host-guest interaction that performs a ternary logic operation using an 1H-NMR easy to read response output is described here. Selenoureas are very versatile receptors for anion binding, capable of forming both mono- and bi-coordinated adducts at room temperature in solution.

A Convenient Synthesis of Mono-, N,N'-Di-, and Tri-substituted Selenoureas from Methyl Carbamimidothioates (S-Methylpseudothioureas)

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