84936-70-9

Basic information

• Product Name: methyl (3β,8β,9α)-1-benzoyl-2,3-dihydro-9-hydroxy-6-methylergoline-8-carboxylate
• CAS NO: 84936-70-9
• Molecular Weight: 406.481
• Mol File: 84936-70-9.mol

Chemical Properties

• CAS DataBase Reference: methyl (3β,8β,9α)-1-benzoyl-2,3-dihydro-9-hydroxy-6-methylergoline-8-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl (3β,8β,9α)-1-benzoyl-2,3-dihydro-9-hydroxy-6-methylergoline-8-carboxylate(84936-70-9)
• EPA Substance Registry System: methyl (3β,8β,9α)-1-benzoyl-2,3-dihydro-9-hydroxy-6-methylergoline-8-carboxylate(84936-70-9)

Safety Data

• Hazardous Substances Data: 84936-70-9(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 84936-69-6 C₂₄H₂₆N₂O₄ 
• 51867-06-2 1-benzoyl-1,2,2a,3-tetrahydrobenzindol-4-(5H)-one 
• 98570-37-7 C₁₇H₂₀N₂O 
• 84936-68-5 (3aβ,5aβ,6aβ,11bα,11cβ)-8-benzoyl-3a,4,5,5a,6,6a,7,8,11b,11c-decahydro-5-methylfuro<3,2-c>indolo<4,3-fg>quinoline 
• 84936-67-4 (3aβ,5aβ,6aβ,11bα,11cβ)-8-benzoyl-5,5a,6,6a,7,8,11b,11c-octahydro-5-methylfuro<3,2-c>indolo<4,3-fg>quinolin-4(3aH)-one 
• 98-88-4 benzoyl chloride 
• 91421-20-4 N-(1-benzoyl-1,2,2a,3-tetrahydrobenzindol-4-yl)-N-methylfuran-3-carboxamide 
• 84936-72-1 (5aS,6aR,9S,10S,10aR)-4-Benzoyl-10-hydroxy-7-methyl-4,5,5a,6,6a,7,8,9,10,10a-decahydro-indolo[4,3-fg]quinoline-9-carbaldehyde 

Downstream Products

• 62630-94-8 methyl (3β)-1-benzoyl-1,2-dihydrolysergate 
• 62592-69-2 methyl (3β)-1-benzoyl-2,3-dihydroisolysergate 

Relevant articles and documents

Photocyclisation of Enamides. Part 24. Total Synthesis of (+/-)-Isofumigaclavine B and (+/-)-Lysergic Acid

Total syntheses of two ergoline-types of alkaloids, (+/-)-isofumigaclavine B (14) (for the first time) and methyl (+/-)-lysergate (21) and methyl (+/-)-isolysergate (22), via a route involving reductive photocyclisation of the enamide (2) followed by glyc

A NEW SYNTHESIS OF (+/-)-LYSERGIC ACID

Reductive photocyclization of the enamide (2) followed by the ring opening of the resulting dihydrofuran derivative (4) completed a new total synthesis of (+/-)-lysergic acid.