874916-40-2

Basic information

• Product Name: 1H-Indolizino[8,7-b]indol-1-one, 2,3,5,6,11,11b-hexahydro-11b-methyl-11-(phenylmethyl)-
• CAS NO: 874916-40-2
• Molecular Formula: C22H22N2O
• Molecular Weight: 330.429
• Mol File: 874916-40-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1H-Indolizino[8,7-b]indol-1-one, 2,3,5,6,11,11b-hexahydro-11b-methyl-11-(phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indolizino[8,7-b]indol-1-one, 2,3,5,6,11,11b-hexahydro-11b-methyl-11-(phenylmethyl)-(874916-40-2)
• EPA Substance Registry System: 1H-Indolizino[8,7-b]indol-1-one, 2,3,5,6,11,11b-hexahydro-11b-methyl-11-(phenylmethyl)-(874916-40-2)

Safety Data

• Hazardous Substances Data: 874916-40-2(Hazardous Substances Data)

Upstream product

• 15741-71-6 N-phthalimidotryptamine 
• 4307-98-6 N-benzyltryptamine 
• 61-54-1 tryptamine 
• 874916-37-7 2-(2-(1-benzyl-1H-indol-3-yl)ethyl)isoindoline-1,3-dione 
• 874916-38-8 3-[2-(1-benzyl-1H-indol-3-yl)ethylamino]propionic acid methyl ester 
• 874916-39-9 9-benzyl-2-(2-methoxycarbonylethyl)-1-methyl-2,3,4,9-tetrahydro-1H-β-carboline-1-carboxylic acid methyl ester 

Relevant articles and documents

Facile construction of the pentacyclic framework of subincanadine B. Synthesis of 20-deethylenylated subincanadine B and 19,20-dihydrosubincanadine B

(Chemical Equation Presented) We describe a facile approach for effectively constructing the pentacyclic framework of subincanadine B. The seven-step assembly of tetracyclic ketone 14 featured Michael addition, Pictet-Spengler cyclization, and Dieckmann condensation. From this key ketone intermediate, two analogues of subincanadine B, i.e., 20-deethylenylated subincanadine B (27) and 19,20-dihydrosubincanadine B (31), were synthesized in four steps, respectively.