372964-07-3

Basic information

• Product Name: 7-(diethylamino)-N-{5-[4-(1-hydroxyethyl)-2-methoxy-5-nitrophenoxy]pentyl}-2-oxo-2H-[1]benzopyran-3-carboxamide
• Synonyms: 7-(diethylamino)-N-{5-[4-(1-hydroxyethyl)-2-methoxy-5-nitrophenoxy]pentyl}-2-oxo-2H-[1]benzopyran-3-carboxamide
• CAS NO: 372964-07-3
• Molecular Weight: 541.601
• Mol File: 372964-07-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 7-(diethylamino)-N-{5-[4-(1-hydroxyethyl)-2-methoxy-5-nitrophenoxy]pentyl}-2-oxo-2H-[1]benzopyran-3-carboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: 7-(diethylamino)-N-{5-[4-(1-hydroxyethyl)-2-methoxy-5-nitrophenoxy]pentyl}-2-oxo-2H-[1]benzopyran-3-carboxamide(372964-07-3)
• EPA Substance Registry System: 7-(diethylamino)-N-{5-[4-(1-hydroxyethyl)-2-methoxy-5-nitrophenoxy]pentyl}-2-oxo-2H-[1]benzopyran-3-carboxamide(372964-07-3)

Safety Data

• Hazardous Substances Data: 372964-07-3(Hazardous Substances Data)

Upstream product

• 372964-05-1 7-(diethylamino)-N-(5-hydroxypentyl)-2-oxo-2H-[1]benzopyran-3-carboxamide 
• 159873-64-0 (R,S)-1-[4',5'-(methylenedioxy)-2'-nitrophenyl]ethanol 
• 50995-74-9 7-(diethylamino)coumarin-3-carboxylic acid 
• 28705-46-6 ethyl 7-diethylaminocoumarin-3-carboxylate 
• 17754-90-4 4-(Diethylamino)salicylaldehyde 
• 56136-84-6 methyl 3,4-(methylenedioxy)-6-nitrophenyl ketone 
• 3162-29-6 1-(benzo[d][1,3]dioxol-6-yl)ethanone 
• 182122-17-4 4-(1-hydroxyethyl)-2-methoxy-5-nitrophenol 
• 372964-06-2 N-(5-bromopentyl)-7-(diethylamino)-2-oxo-2H-[1]benzopyran-3-carboxamide 

Downstream Products

• 372964-08-4 5'-O-{[1-(4-{5-[7-(diethylamino)-2-oxo-2H-[1]benzopyran-3-carboxamido]pentyloxy}-5-methoxy-2-nitrophenyl)-ethoxy]carbonyl}thymidine 

Relevant articles and documents

Protection and labelling of thymidine by a fluorescent photolabile group

A fluorescent photolabile group including coumarin and MeNPOC moieties was synthesized to protect 5′-OH terminal function of thymidine (T). Its photochemical and photophysical properties were studied, in particular the photocleavage (photodeprotection under a 365-nm irradiation) is only lowered by a factor of two by addition of the fluorophore. Fluorescence properties of the coumarin probe are not changed upon irradiation, which is satisfactory for the application required, i.e., in situ synthesis of DNA microarrays.