6124-02-3

Basic information

• Product Name: Selenourea, phenyl-
• CAS NO: 6124-02-3
• Molecular Formula: C7H8N2Se
• Molecular Weight: 199.114
• Mol File: 6124-02-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Selenourea, phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Selenourea, phenyl-(6124-02-3)
• EPA Substance Registry System: Selenourea, phenyl-(6124-02-3)

Safety Data

• Hazardous Substances Data: 6124-02-3(Hazardous Substances Data)

Upstream product

• 622-34-4 1-phenylcyanamide 
• 62-53-3 aniline 
• 622-44-6 phenylcarbonimidic dichloride 
• 103-85-5 monophenylthiourea 
• 3898-07-5 N-phenyl-benzamidine 
• 27806-84-4 S-methyl-N-phenylisothiourea hydroiodide 
• 2040-68-8 N'-Phenyl-N-benzoylselenoharnstoff 
• 4426-68-0 phenyl isoselenocyanate 

Downstream Products

• 63200-79-3 (5-nitro-4-phenyl-selenazol-2-yl)-phenyl-amine 
• 19765-37-8 2-phenylamino-4-methyl-1,3-selenazole 
• 19765-46-9 2-phenylamino-4-(4-tolyl)-1,3-selenazole 
• 127348-92-9 2,3,5-Trichloro-6-(2-phenylamino-selenazol-5-yl)-benzene-1,4-diol 
• 5467-78-7 fenamole 
• 2433-53-6 3-(phenylamino)-2H-1,2,4-triazole 
• 19765-35-6 2-phenylamino-1,3-selenazole 
• 19761-59-2 2-phenylamino-4-(4-methoxyphenyl)-1,3-selenazole 
• 622-34-4 1-phenylcyanamide 
• 19761-67-2 N-[4-(4-nitro-phenyl)-selenazol-2-yl]-N-phenyl-acetamide 
• 19761-61-6 N-[4-(4-methoxy-phenyl)-selenazol-2-yl]-N-phenyl-acetamide 
• 19761-64-9 N-[4-(4-chloro-phenyl)-selenazol-2-yl]-N-phenyl-acetamide 

Relevant articles and documents

Synthesis, reactivity and antimicrobial activity of a series of 2-arylamino-1,3-selenazoles

A series of 2-arylamino-1,3-selenazoles was synthesized and their reactivity was studied. The 2-arylamino-1,3-selenazoles and their reaction products were characterized by various spectroscopic methods and X-ray diffraction. In addition, the antimicrobial

Synthesis of cyanamides from isoselenocyanates promoted by recyclable ionic liquid-supported (diacetoxyiodo)benzene

One-pot synthesis of cyanamides from isoselenocyanates through deselenisation promoted by ionic liquid-supported hypervalent iodine(III) reagent 1-(4-diacetoxyiodobenzyl)-3-methylimidazolium tetrafluoroborate [dibmim BF4 was developed. This approach provided a simple, mild and environmentally benign way to construct cyanamides in good yields. Moreover, powder Se and dibmim + BF4 could be easily recycled. It was the first example of [dibmim] + [BF4- to be used as a deselenising agent.