77612-47-6

Upstream product

• 54955-24-7 N-cyclohexyl-N-nitrosoaniline 
• 1821-36-9 N-phenyl-2-cyclohexylamine 
• 108-85-0 1-bromocyclohexane 
• 100-63-0 phenylhydrazine 

Downstream Products

• 847355-61-7 9-cyclohexyl-2,3,4,9-tetrahydro-1H-carbazole 
• 86759-72-0 N'-[1-Benzo[1,3]dioxol-5-yl-meth-(E)-ylidene]-N-cyclohexyl-N-phenyl-hydrazine 
• 1821-36-9 N-phenyl-2-cyclohexylamine 
• 2834-92-6 1-amino-2-naphthol 
• 77612-48-7 1-Cyclohexyl-1-phenyl-2-(3-sulfamoyl-4-chlorobenzoyl)-hydrazine 

Relevant academic research and scientific papers

An efficient synthesis of 1,1-disubstituted hydrazines

1,1-disubstituted hydrazines were prepared from the corresponding 1,1-disubstituted ureas by means of the Hofmann rearrangement reaction. The yields were fairly good, except from the ureas susceptible to oxidation, and thus the present method represents an additional and efficient procedure for the synthesis of 1,1-disubstituted hydrazines.

Amino-benzamides

Compounds of the formula STR1 wherein: Ar and Ar' are independently alicyclic aryl or heterocyclic aryl groups; R1 is a substituent replacing a hydrogen on the ring and is independently hydroxy, alkyl, alkoxy, halogen, nitro, amino, monoalkyl-a