79664-57-6

Basic information

• Product Name: N-formyl-1,2-dihydrorenierone
• Synonyms: N-formyl-1,2-dihydrorenierone
• CAS NO: 79664-57-6
• Molecular Weight: 345.352
• Mol File: 79664-57-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-formyl-1,2-dihydrorenierone(CAS DataBase Reference)
• NIST Chemistry Reference: N-formyl-1,2-dihydrorenierone(79664-57-6)
• EPA Substance Registry System: N-formyl-1,2-dihydrorenierone(79664-57-6)

Safety Data

• Hazardous Substances Data: 79664-57-6(Hazardous Substances Data)

Upstream product

• 77607-84-2 (7-methoxy-6-methyl-8-nitro-1-isoquinolyl)methanol 
• 98498-44-3 (N-formyl-5,7,8-trimethoxy-6-methyl-1,2,3,4-tetrahydro-1-isoquinolyl)methyl angelate 
• 124867-50-1 N-formyl-1-hydroxymethyl-5,7,8-trimethoxy-6-methyl-1,2,3,4-tetrahydroisoquinoline 
• 124909-66-6 (N-formyl-7-methoxy-6-methyl-5,8-dioxo-1,2,3,4,5,8-hexahydro-1-isoquinolyl)methanol 
• 98498-42-1 1-Hydroxymethyl-6-methyl-5,7,8-trimethoxy-1,2,3,4-tetrahydroisoquinoline 
• 110828-13-2 2,2-dimethoxy-N-(2,3,5-trimethoxy-4-methylbenzyl)-N-tosylethylamine 
• 110828-15-4 N-benzoyl-1-cyano-5,7,8-trimethoxy-6-methyl-1,2-dihydroisoquinoline 
• 110828-14-3 5,7,8-trimethoxy-6-methyl-N-tosyl-1,2-dihydroisoquinoline 
• 94893-31-9 2,2-dimethoxy-N-(2,3,5-trimethoxy-4-methylbenzylidene)ethylamine 
• 86433-68-3 (5,7,8-trimethoxy-6-methyl-1-isoquinolyl)methyl benzoate 
• 86433-67-2 5,7,8-trimethoxy-6-methyl-isoquinoline 
• 77515-78-7 1-Hydroxymethyl-6-methyl-5,7,8-trimethoxyisoquinoline 
• 35660-94-7 (Z)-2-methyl-2-butenoyl chloride 
• 123641-95-2 renieramycin E 

Downstream Products

• 73777-65-8 (5,8-dihydro-7-methoxy-6-methyl-5,8-dioxo-1-isoquinolinyl)methyl (2Z)-2-methyl-2-butenoate 

Relevant articles and documents

Chemistry of renieramycins. Part 6: Transformation of renieramycin M into jorumycin and renieramycin J including oxidative degradation products, mimosamycin, renierone, and renierol acetate

The transformation of renieramycin M (1m) into renieramycin J (1j) and jorumycin (2) is presented along with the results of antiproliferative assay data. The chemical stability and the oxidative degradation of 2 and renieramycin E (1e) to generate simple isoquinoline alkaloids, such as mimosamycin (7), renierol acetate (12), and renierone (8) are also described.

Synthesis of isoquinolinequinone antibiotics from a marine sponge Reniera sp.

Synthesis of two isoquinolinequinone antibiotics, 7-methoxy-1,6-dimethyl-5,8-dihydroisoquinoline-5,8-dione and N-formyl-1,2-dihydrorenierone, isolated from a marine sponge Reniera sp., are described.