1219380-72-9

Basic information

• Product Name: N,N'-di-tert-butoxycarbonylpiperazic acid
• Synonyms: N,N'-di-tert-butoxycarbonylpiperazic acid
• CAS NO: 1219380-72-9
• Molecular Weight: 330.381
• Mol File: 1219380-72-9.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 422.0±55.0 °C(Predicted)
• Density: 1.200±0.06 g/cm3(Predicted)
• CAS DataBase Reference: N,N'-di-tert-butoxycarbonylpiperazic acid(CAS DataBase Reference)
• NIST Chemistry Reference: N,N'-di-tert-butoxycarbonylpiperazic acid(1219380-72-9)
• EPA Substance Registry System: N,N'-di-tert-butoxycarbonylpiperazic acid(1219380-72-9)

Safety Data

• Hazardous Substances Data: 1219380-72-9(Hazardous Substances Data)

Upstream product

• 1161001-03-1 di-tert-butyl 3-methyl hexahydropyridazine-1,2,3-tricarboxylate 
• 336817-83-5 N,N'-di-tert-butoxycarbonylpiperazic acid ethyl ester 
• 1618700-88-1 1,2-di-tert-butyl 3,3-dibenzyl hexahydropyridazine-1,2,3,3-tetracarboxylate 

Downstream Products

• 24182-11-4 (3RS)-piperazic acid 
• 1618700-72-3 3-(2-(tert-butoxycarbonylamino)-3-phenylpropyl) 1,2-di-tert-butyl hexahydropyridazine-1,2,3-tricarboxylate 
• 1618700-60-9 3-(2-(tert-butoxycarbonylamino)-3-phenylpropyl) 1,2-di-tert-butyl hexahydropyridazine-1,2,3-tricarboxylate 
• 1618700-63-2 (S)-di-tert-butyl 3-((S)-1-methoxy-1-oxo-3-phenylpropan-2-ylcarbamoyl)hexahydropyridazine-1,2-dicarboxylate 
• 1618700-75-6 (R)-di-tert-butyl 3-((S)-1-methoxy-1-oxo-3-phenylpropan-2-ylcarbamoyl)hexahydropyridazine-1,2-dicarboxylate 
• 72120-54-8 1-(benzyloxycarbonyl)hexahydro-3-pyridazinecarboxylic acid 
• 174497-80-4 methyl (3R)-N,N'-bis-(t-butoxycarbonyl)hexahydropyridazine-3-carboxylate 
• 222556-21-0 (S)-tetrahydro-pyridazine-1,2,3-tricarboxylic acid 1,2-di-tert-butyl ester 3-methyl ester 

Relevant articles and documents

Improved synthesis of cyclic α -hydrazino acids of five- to nine-membered rings and optical resolution of 5,6,7-membered ring hydrazino acids

GRAPHICAL ABSTRACT Synthesis of cyclic α-hydrazino acids of five- to nine-membered rings has been described. Di-tert-butyl or dibenzyl malonate was used as starting materials instead of diethyl malonate, which was used in our first report. Deprotection of