194664-25-0

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 194664-23-8 C₁₅H₁₃N₃O₄S 
• 49584-26-1 p-cyanobenzenesulfonyl chloride 
• 5331-43-1 N-benzyloxycarbonyl-hydrazine 
• 1538-75-6 2,2-dimethylpropanoic anhydride 

Downstream Products

• 194664-28-3 C₂₅H₃₁N₃O₆S 
• 194664-26-1 1-benzyloxycarbonyl-2-tert-butyloxycarbonyl-1-(4-chlorobenzyl)-2-(4-cyanobenzenesulfonyl)-hydrazine 
• 194664-27-2 1-benzyloxycarbonyl-2-tert-butyloxycarbonyl-2-(4-cyanobenzenesulfonyl)-1-(4-methoxybenzyl)-hydrazine 
• 192320-28-8 C₂₇H₂₇N₃O₆S 
• 194664-40-9 C₂₅H₃₃N₃O₆ 
• 194664-33-0 C₂₄H₃₀N₂O₆ 
• 194664-35-2 C₂₁H₂₅ClN₂O₄ 
• 194664-30-7 C₂₁H₂₆N₂O₅ 
• 194664-45-4 N-Benzyl-N'-(4-fluoro-benzoyl)-N'-methyl-hydrazinecarboxylic acid benzyl ester 
• 1027411-30-8 N'-Benzoyl-N-(4-chloro-benzyl)-N'-methyl-hydrazinecarboxylic acid benzyl ester 
• 194664-32-9 C₂₁H₂₆N₂O₄ 
• 194664-29-4 C₂₀H₂₃ClN₂O₄ 
• 194664-42-1 (N'-Benzyl-N'-benzyloxycarbonyl-hydrazino)-acetic acid ethyl ester 
• 194664-31-8 C₁₈H₂₈N₂O₄ 

Relevant academic research and scientific papers

Cyclic Voltammetry Studies on Substituted Arenesulfonylhydrazides

The cathodic potential of the sulfonyl functions (R; R=tosyl, 4-cyanobenzenesulfonyl, 1- and 2-naphthalenesulfonyl) of 23 arenesulfonylhydrazides RSO2NR1-NR2R3, with up to 3 Boc and/or Z groups on their nitrogens, have bee

Stepwise synthesis of tetrasubstituted hydrazines

A new triprotected hydrazine reagent has been made and applied in alkylation/acylation reactions for stepwise synthesis of tetrasubstituted derivatives in high purity and yield.