41019-37-8

Basic information

• Product Name: 5-(3-NITROPHENYL)FURAN-2-CARBOXYLIC ACID METHYL ESTER
• Synonyms: 5-(3-NITROPHENYL)FURAN-2-CARBOXYLIC ACID METHYL ESTER;RARECHEM AL BF 0713;5-(3-nitrophenyl)-2-Furancarboxylic acid methyl ester
• CAS NO: 41019-37-8
• Molecular Formula: C₁₂H₉NO₅
• Molecular Weight: 247.2
• Mol File: 41019-37-8.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 5-(3-NITROPHENYL)FURAN-2-CARBOXYLIC ACID METHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(3-NITROPHENYL)FURAN-2-CARBOXYLIC ACID METHYL ESTER(41019-37-8)
• EPA Substance Registry System: 5-(3-NITROPHENYL)FURAN-2-CARBOXYLIC ACID METHYL ESTER(41019-37-8)

Safety Data

• Hazardous Substances Data: 41019-37-8(Hazardous Substances Data)

Upstream product

• 2527-99-3 methyl 5-bromo-2-furoate 
• 13331-27-6 m-nitrobenzene boronic acid 
• 13130-13-7 5-(3-nitro-phenyl)-furan-2-carboxylic acid 
• 74-88-4 methyl iodide 
• 67-56-1 methanol 
• 61941-87-5 5-(3-nitrophenyl)furan-2-carbonyl chloride 
• 98-01-1 furfural 
• 611-13-2 2-furoic acid methyl ester 
• 99-09-2 3-nitro-aniline 

Downstream Products

• 54023-06-2 5-(3-amino-phenyl)-furan-2-carboxylic acid methyl ester 
• 528885-24-7 5-(3-(2-(5-cyclohexyl-1-(3,3-dimethyl-2-oxo-butyl)-2-oxo-1,2-dihydro-3H-1,3,4-benzotriazepin-3-yl)-acetylamino)-phenyl)-furan-2-carboxylic acid 
• 942232-15-7 C₃₄H₃₈N₄O₆ 
• 13130-13-7 5-(3-nitro-phenyl)-furan-2-carboxylic acid 

Relevant articles and documents

Carbon–Carbon Bond Formation for the Synthesis of 5-Aryl-2-Substituted Furans Catalyzed by K3[Fe(CN)6]

An efficient method for the carbon–carbon bond formation at C-5 position of 2-substituted furans to provide a range of π-diverse 5-aryl-2-substituted furan derivatives in 58–80% yield has been reported. The method employs several advantages such as use of catalytic amount of K3[Fe(CN)6] under mild conditions and short reaction time with high yields. Also, a variety of anilines with a variety of functional groups can be employed for the synthesis of 5-aryl-2-substituted furans. Graphic Abstract: [Figure not available: see fulltext.]

Synthesis and SAR of 5-aryl-furan-2-carboxamide derivatives as potent urotensin-II receptor antagonists

The synthesis and biological evaluation as potential urotensin-II receptor antagonists of a series of 5-arylfuran-2-carboxamide derivatives 1, bearing a 4-(3-chloro-4-(piperidin-4-yloxy)benzyl)piperazin-1-yl group, are described. The results of a systemat

AMINO ACIDS

Compounds of formula (I): Z’ -CO-A-B-NH-Z (I) wherein: Z is H or an amino protecting group; Z’ is OH, a protected or activated hydroxyl group or C1; A is an optionally substituted C5-6 arylene group; and B is an optionally substituted C5-6 arylene group.