6124-02-3

Upstream product

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

Downstream Products

• 23287-09-4 N-acetyl-N'-phenylselenourea 
• 19765-35-6 2-phenylamino-1,3-selenazole 
• 63200-79-3 (5-nitro-4-phenyl-selenazol-2-yl)-phenyl-amine 
• 19761-70-7 (4,5-dimethyl-selenazol-2-yl)-phenyl-amine 
• 19765-37-8 2-phenylamino-4-methyl-1,3-selenazole 
• 19765-43-6 2-phenylamino-4-phenyl-1,3-selenazole 
• 66497-19-6 2-anilino-4-oxo-4H-[1,3]selenazine-6-carboxylic acid methyl ester 
• 19761-73-0 2-anilino-4-methyl-selenazole-5-carboxylic acid ethyl ester 
• 19761-59-2 2-phenylamino-4-(4-methoxyphenyl)-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 
• 66497-38-9 2-anilino-4-oxo-5,6-dihydro-4H-[1,3]selenazine-6-carboxylic acid methyl ester 
• 622-34-4 1-phenylcyanamide 
• 5467-78-7 fenamole 

Relevant academic research and scientific papers

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

A novel and convenient synthesis of 3-amino-2H-1,2,4-triazoles from isoselenocyanates and hydrazine hydrate

A novel and convenient one-pot synthesis of 3-amino-2H-1,2,4-triazoles from two molecules of isoselenocyanates and hydrazine hydrate via cyclodeselenisation was developed. Various 3-amino-2H-1,2,4-triazoles were obtained in moderate to good yields (33-45%

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.