64512-89-6

Upstream product

• 870-46-2 t-butoxycarbonylhydrazine 
• 1885-14-9 phenyl chloroformate 
• 6627-89-0 tert-butyl phenyl carbonate 

Downstream Products

• 135441-04-2 t-butyl phenyl azodiformate 
• 1391719-83-7 phenyl N-[(tert-butoxycarbonylamino)carbamoylamino]carbamate 
• 64512-82-9 tert-butyl 2-(benzylcarbamoyl)hydrazinecarboxylate 
• 20605-43-0 phenyl hydrazinecarboxylate 
• 64512-90-9 tert-butyl N-(hydrazinecarbonylamino)carbamate 

Relevant academic research and scientific papers

Carbonylhydrazide-based molecular tongs inhibit wild-type and mutated HIV-1 protease dimerization

We have designed and synthesized new molecular tongs based on a rigid naphthalene scaffold and evaluated their antidimer activity on HIV-1 protease (PR). We inserted carbonylhydrazide and oligohydrazide (azatide) fragments into their peptidomimetic arms t

SYNTHESIS OF A NON-SYMMETRIC AZODICARBONYL COMPOUND AND ITS REGIOSELECTIVE REACTION WITH ORGANOMETALLIC REAGENTS

The non-symmetric azodicarbonyl compound 7 reacted with R-M/Lewis acid regioselectively at the nitrogen atom attached to the amide group giving 9, whereas it reacted with R-M at the nitrogen atom attached to the ester group producing 8 in high yield.