15856-35-6

Basic information

• Product Name: ethyl 5-aminofuran-2-carboxylate
• Synonyms: 2-furancarboxylic acid, 5-amino-, ethyl ester; Ethyl 5-amino-2-furancarboxylate
• CAS NO: 15856-35-6
• Molecular Formula: C₇H₉NO₃
• Molecular Weight: 155.1513
• Mol File: 15856-35-6.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 288°C at 760 mmHg
• Flash Point: 128°C
• Density: 1.203g/cm³
• Vapor Pressure: 0.0024mmHg at 25°C
• Refractive Index: 1.52
• CAS DataBase Reference: ethyl 5-aminofuran-2-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 5-aminofuran-2-carboxylate(15856-35-6)
• EPA Substance Registry System: ethyl 5-aminofuran-2-carboxylate(15856-35-6)

Safety Data

• Hazardous Substances Data: 15856-35-6(Hazardous Substances Data)

Upstream product

• 943-37-3 5-nitrofuran-2-carboxylic acid ethyl ester 

Downstream Products

• 1207827-92-6 ethyl 6-hydroxy-6-(trifluoromethyl)-6H-chromeno[4,3-b]furo[3,2-e]pyridine-9-carboxylate 
• 1207827-83-5 ethyl 5-salicyloyl-6-(trifluoromethyl)furo[2,3-b]pyridine-2-carboxylate 
• 6562-74-9 ethyl 5-aminofuro[2,3-b]pyridine-2-carboxylate 
• 6563-65-1 5-nitro-furo[2,3-b]pyridine-2-carboxylic acid 
• 74134-50-2 1-(5-ethoxycarbonyl-2-furyl)-2-(4-nitrophenyl)aziridine 
• 74134-49-9 ethyl 5-(4-nitrobenzylideneamino)furoate 
• 6563-64-0 ethyl 5-nitrofuro[2,3-b]pyridine-2-carboxylate 

Relevant articles and documents

Disubstituted aryl and heteroaryl imines having retinoid-like biological activity

Compounds of the formula STR1 wherein the R 1 groups independently are hydrogen, lower alkyl, or two geminal R 1 groups jointly represent an oxo ( O) or a thio ( S) group; R 2 is hydrogen or lower alkyl, or halogen; M is or --N CR 4 -- or --R 4 C N-- where R 4 is hydrogen or lower alkyl; X is C(R 1) 2 ; Y is phenyl optionally substituted with an R 3 group which is lower alkyl or halogen; A is (CH 2) n where n is 0-5, lower branched chain alkyl, cycloalkyl, alkenyl, alkynyl; B is hydrogen, COOH or a pharmaceutically acceptable salt thereof, COOR 8, CONR 9 R 10, --CH 2 OH, CH 2OR 11, CH 2 OCOR 11, CHO, CH(OR 12) 2, CHOR 13 O, --COR 7, CR 7 (OR 12) 2, or CR 7 OR 13 O, where R 7 is an alkyl, cycloalkyl or alkenyl group containing 1 to 5 carbons, R 8 is an alkyl group of 1 to 10 carbons, or a cycloalkyl group of 5 to 10 carbons, or R 8 is phenyl or lower alkylphenyl, R 9 and R 10 independently are hydrogen, an alkyl group of 1 to 10 carbons, or a cycloalkyl group of 5-10 carbons, or phenyl or lower alkylphenyl, R 11 is lower alkyl, phenyl or lower alkylphenyl, R 12 is lower alkyl, and R 13 is divalent alkyl radical of 2-5 carbons have retinoid-like biological activity.