1333429-92-7

Basic information

• Product Name: (2R,3R,4R)-tert-butyl 6-methoxy-3-nitro-4-(2-oxoethyl)-2-phenyl-3,4-dihydro-1H-carbazole-9(2H)-carboxylate
• Synonyms: (2R,3R,4R)-tert-butyl 6-methoxy-3-nitro-4-(2-oxoethyl)-2-phenyl-3,4-dihydro-1H-carbazole-9(2H)-carboxylate
• CAS NO: 1333429-92-7
• Molecular Weight: 464.518
• Mol File: 1333429-92-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2R,3R,4R)-tert-butyl 6-methoxy-3-nitro-4-(2-oxoethyl)-2-phenyl-3,4-dihydro-1H-carbazole-9(2H)-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3R,4R)-tert-butyl 6-methoxy-3-nitro-4-(2-oxoethyl)-2-phenyl-3,4-dihydro-1H-carbazole-9(2H)-carboxylate(1333429-92-7)
• EPA Substance Registry System: (2R,3R,4R)-tert-butyl 6-methoxy-3-nitro-4-(2-oxoethyl)-2-phenyl-3,4-dihydro-1H-carbazole-9(2H)-carboxylate(1333429-92-7)

Safety Data

• Hazardous Substances Data: 1333429-92-7(Hazardous Substances Data)

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 6260-86-2 5-methoxy-2-methyl-1H-indole-3-carbaldehyde 
• 1333429-74-5 tert-butyl 3-formyl-5-methoxy-2-methyl-1H-indole-1-carboxylate 
• 1333429-69-8 C₁₈H₂₀N₂O₃ 
• 102-96-5 (2-nitroethenyl)benzene 
• 1333429-63-2 (E)-tert-butyl 5-methoxy-2-methyl-3-(3-oxoprop-1-en-1-yl)-1H-indole-1-carboxylate 

Downstream Products

• 1333430-15-1 C₂₆H₃₀N₂O₆ 

Relevant articles and documents

Asymmetric catalysis of Diels-Alder reactions with in situ generated heterocyclic ortho -quinodimethanes

The Diels-Alder reaction is probably the most powerful technology in the synthetic repertoire for single-step constructions of complex chiral molecules. The synthetic power of this fundamental pericyclic transformation has greatly increased with the emerg