3084-13-7

Basic information

• Product Name: 2,4,6-Cycloheptatrien-1-one, 2-hydroxy-5-nitro-
• Synonyms: 5-Nitrotropolon;2,4,6-Cycloheptatrien-1-one,2-hydroxy-5-nitro;5-nitrotropolene;5-nitrotropolone;2-hydroxy-5-nitro-2,4,6-cycloheptatrien-1-one;2-Hydroxy-5-nitro-cyclohepta-2,4,6-trienone
• CAS NO: 3084-13-7
• Molecular Formula: C7H5NO4
• Molecular Weight: 167.121
• Mol File: 3084-13-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2,4,6-Cycloheptatrien-1-one, 2-hydroxy-5-nitro-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,6-Cycloheptatrien-1-one, 2-hydroxy-5-nitro-(3084-13-7)
• EPA Substance Registry System: 2,4,6-Cycloheptatrien-1-one, 2-hydroxy-5-nitro-(3084-13-7)

Safety Data

• Hazardous Substances Data: 3084-13-7(Hazardous Substances Data)

Upstream product

• 533-75-5 2-hydroxy-2,4,6-cycloheptatrien-1-one 
• 544-25-2 Cyclohepta-1,3,5-triene 
• 7664-93-9 sulfuric acid 
• 52003-24-4 cyclohepta-3,6-diene-1,2,5-trione-5-oxime 
• 7722-84-1 dihydrogen peroxide 
• 2297-94-1 5-nitrosotropolone 

Downstream Products

• 14628-90-1 2-methoxy-5-nitro-cycloheptatrien-1-one 
• 3084-17-1 5-chloro-5-tropolone 
• 192327-43-8 di(O,O-5-nitrotropolonato)tri(phenyl)bismuth(V) 
• 15852-34-3 2,5-dihydroxycyclohepta-2,4,6-trien-1-one 
• 60423-21-4 2-methoxy-5-(2',3',4'-trimethoxyphenyl)-2,4,6-cycloheptatrien-1-one 

Relevant articles and documents

TROPOLONE DERIVATIVES AND TAUTOMERS THEREOF FOR IRON REGULATION IN ANIMALS

Disclosed are a series of compounds or their tautomers having a general structure represented by Formula (la), (lb), (Ila), (lIb), or (lIc) and pharmaceutically acceptable salts thereof. The present disclosure also relates to pharmaceutical compositions comprising said compounds or tautomers. The present disclosure further relates to a method of treating a disease or condition associated with iron dysregulation or dysfunctional iron homeostasis comprising administering to a subject in need thereof a therapeutically effective amount of Formula (la), (lb), (Ila), (lIb), or (lIc) compounds or tautomers.

Improved and highly versatile synthesis of 5-aryltropones

The use of 5-iodo-2-methoxytropone in palladium(0)-catalyzed coupling reactions with a variety of arylboronic acids has resulted in significantly improved reaction yields and times for a sterically and electronically diverse series of novel 5-aryltropones