625123-60-6

Basic information

• Product Name: 2-(3-{4-[(2S,4R)-2-(Bis-ethylsulfanyl-methyl)-4-hydroxy-pyrrolidine-1-carbonyl]-2-methoxy-5-nitro-phenoxy}-propyl)-benzo[de]isoquinoline-1,3-dione
• Synonyms: 2-(3-{4-[(2S,4R)-2-(Bis-ethylsulfanyl-methyl)-4-hydroxy-pyrrolidine-1-carbonyl]-2-methoxy-5-nitro-phenoxy}-propyl)-benzo[de]isoquinoline-1,3-dione
• CAS NO: 625123-60-6
• Molecular Weight: 653.777
• Mol File: 625123-60-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-(3-{4-[(2S,4R)-2-(Bis-ethylsulfanyl-methyl)-4-hydroxy-pyrrolidine-1-carbonyl]-2-methoxy-5-nitro-phenoxy}-propyl)-benzo[de]isoquinoline-1,3-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3-{4-[(2S,4R)-2-(Bis-ethylsulfanyl-methyl)-4-hydroxy-pyrrolidine-1-carbonyl]-2-methoxy-5-nitro-phenoxy}-propyl)-benzo[de]isoquinoline-1,3-dione(625123-60-6)
• EPA Substance Registry System: 2-(3-{4-[(2S,4R)-2-(Bis-ethylsulfanyl-methyl)-4-hydroxy-pyrrolidine-1-carbonyl]-2-methoxy-5-nitro-phenoxy}-propyl)-benzo[de]isoquinoline-1,3-dione(625123-60-6)

Safety Data

• Hazardous Substances Data: 625123-60-6(Hazardous Substances Data)

Upstream product

• 81-83-4 1,8-Naphthalimide 
• 625123-59-3 (4R)-hydroxy-(2S)-N-[4-(3-bromopropoxy)-5-methoxy-2-nitrobenzoyl]-pyrrolidine-2-carboxaldehyde diethyl thioacetal 
• 625123-58-2 (2S,4R)-1-[4-(3-Bromo-propoxy)-5-methoxy-2-nitro-benzoyl]-4-(tert-butyl-dimethyl-silanyloxy)-pyrrolidine-2-carbaldehyde 
• 625123-57-1 (2S,4R)-1-[4-(3-Bromo-propoxy)-5-methoxy-2-nitro-benzoyl]-4-(tert-butyl-dimethyl-silanyloxy)-pyrrolidine-2-carboxylic acid methyl ester 

Downstream Products

• 625123-61-7 2-(3-{4-[2-(bis-ethylsulfanyl-methyl)-4-oxo-pyrrolidine-1-carbonyl]-2-methoxy-5-nitro-phenoxy}-propyl)-benzo[de]isoquinoline-1,3-dione 

Relevant articles and documents

Synthesis of novel C2 and C2-C8 linked pyrrolo[2,1-c][1,4]benzodiazepine-naphthalimide hybrids as DNA-binding agents

Synthesis of C2 and C2-C8 linked pyrrolobenzodiazepine-naphthalimide hybrids have been prepared that exhibit significant DNA-binding affinity and cytotoxicity.