1425040-20-5

Basic information

• Product Name: tert-butyl 2-(4-chlorophenylcarbamoyl)diazenecarboxylate
• Synonyms: tert-butyl 2-(4-chlorophenylcarbamoyl)diazenecarboxylate
• CAS NO: 1425040-20-5
• Molecular Weight: 283.714
• Mol File: 1425040-20-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: tert-butyl 2-(4-chlorophenylcarbamoyl)diazenecarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl 2-(4-chlorophenylcarbamoyl)diazenecarboxylate(1425040-20-5)
• EPA Substance Registry System: tert-butyl 2-(4-chlorophenylcarbamoyl)diazenecarboxylate(1425040-20-5)

Safety Data

• Hazardous Substances Data: 1425040-20-5(Hazardous Substances Data)

Upstream product

• 78044-32-3 C₁₂H₁₆ClN₃O₃ 
• 104-12-1 p-chlorphenylisocyanate 
• 870-46-2 t-butoxycarbonylhydrazine 

Downstream Products

• 1425040-63-6 (3R,7aS)-2-tert-butyl 6,6-dimethyl 1-((4-chlorophenyl)carbamoyl)-3-ethyl-7,7a-dihydro-1H-cyclopenta[c]pyridazine-2,6,6(3H,5H)-tricarboxylate 
• 1425040-65-8 (3R,7aS)-2-tert-butyl 6,6-dimethyl 1-((4-chlorophenyl)carbamoyl)-3-propyl-7,7a-dihydro-1H-cyclopenta[c]pyridazine-2,6,6(3H,5H)-tricarboxylate 
• 1425040-67-0 (3R,7aS)-2-tert-butyl 6,6-dimethyl 1-((4-chlorophenyl)carbamoyl)-3-isopropyl-7,7a-dihydro-1H-cyclopenta[c]pyridazine-2,6,6(3H,5H)-tricarboxylate 
• 1425040-69-2 (3R,7aS)-2-tert-butyl 6,6-dimethyl 1-((4-chlorophenyl)carbamoyl)-3-phenethyl-7,7a-dihydro-1H-cyclopenta[c]pyridazine-2,6,6(3H,5H)-tricarboxylate 
• 1425040-83-0 (Z)-4-chloro-N-((2R,4aR)-2-methyl-4a,5-dihydro-1H-oxazolo[3,4-b]pyridazin-7(2H)-ylidene)aniline 
• 1425040-75-0 C₁₃H₁₆ClN₃O₂ 
• 1425040-26-1 (3R,6S)-tert-butyl 2-((4-chlorophenyl)carbamoyl)-3,6-dimethyl-2,3-dihydropyridazine-1(6H)-carboxylate 
• 1425040-29-4 (3S,6R)-tert-butyl 2-((4-chlorophenyl)carbamoyl)-3,6-dimethyl-2,3-dihydropyridazine-1(6H)-carboxylate 
• 1425040-35-2 (3R,6R)-tert-butyl 3-(acetoxymethyl)-2-(4-chlorophenylcarbamoyl)-6-ethyl-2,3-dihydropyridazine-1(6H)-carboxylate 
• 1425040-41-0 (3S,6R)-tert-butyl 2-(4-chlorophenylcarbamoyl)-6-(2-hydroxyethyl)-3,4-dimethyl-2,3-dihydropyridazine-1(6H)-carboxylate 
• 1425040-43-2 (3S,8aS)-tert-butyl 1-(4-chlorophenylcarbamoyl)-3-(methoxymethyl)-3,5,6,7,8,8a-hexahydrocinnoline-2(1H)-carboxylate 
• 1425040-49-8 (3aS,5aR)-tert-butyl 5-(4-chlorophenylcarbamoyl)-3,3a,5,5a,6,8-hexahydrodifuro[3,4-c:3',4'-e]pyridazine-4(1H)-carboxylate 
• 1425040-51-2 (3R,7aS)-2-tert-butyl 6,6-diethyl 1-(4-chlorophenylcarbamoyl)-3-methyl-7,7a-dihydro-1H-cyclopenta[c]pyridazine-2,6,6(3H,5H)-tricarboxylate 
• 1425040-71-6 (3S,7aR)-2-tert-butyl 6,6-diethyl 1-(4-chlorophenylcarbamoyl)-3-methyl-7,7a-dihydro-1H-cyclopenta[c]pyridazine-2,6,6(3H,5H)-tricarboxylate 

Relevant articles and documents

Asymmetric hetero-Diels-Alder reaction of diazenes catalyzed by chiral silver phosphate: Water participates in the catalysis and stereocontrol

The chiral silver phosphate was confirmed to efficiently catalyze a highly regio- and enantioselective hetero-Diels-Alder reaction of diazenes to furnish piperazine derivatives in high yields and excellent ee values. DFT calculations revealed that the wat