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Synonyms
NSC54255 | 2-Furoic acid, 5-nitro-, ethyl ester | Ethyl 5-nitro-2-furoate | NSC38652 | NSC-38652 | SCHEMBL1167414 | ethyl 5-nitro-2-furancarboxylate | 4(1H)-Pyrimidinone, 2,6-dimethyl- | ethyl 5-nitrofuran-2-carboxylate | F0191-0153 | BRN 0181268 | 4-Hydr
Specifications Sinónimos
NSC54255 | 2-Furoic acid, 5-nitro-, ethyl ester | Ethyl 5-nitro-2-furoate | NSC38652 | NSC-38652 | SCHEMBL1167414 | ethyl 5-nitro-2-furancarboxylate | 4(1H)-Pyrimidinone, 2, 6-dimethyl- | ethyl 5-nitrofuran-2-carboxylate | F0191-0153 | BRN 0181268 | 4-Hydr
Especificaciones y pureza
≥96%
Condiciones de almacenamiento de almacenamiento
Room temperature
Nombres e identificadores Pubchem Sid 488184528 Sonrisas canónicas CCOC(=O)C1=CC=C(O1)[N+](=O)[O-] IUPAC Name ethyl 5-nitrofuran-2-carboxylate InChIKey JMNXLAQKIHVFIC-UHFFFAOYSA-N INCHI 1S/C7H7NO5/c1-2-12-7(9)5-3-4-6(13-5)8(10)11/h3-4H,2H2,1H3 Isómeros SMILES CCOC(=O)C1=CC=C(O1)[N+](=O)[O-] Peso molecular 185.13 Reaxy-Rn 181268 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=181268&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
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Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Organoheterocyclic compounds Clase Furans Subclass Furoic acid and derivatives Intermediate Tree Nodes Not available Direct Parent Furoic acid esters Alternative Parents Nitrofurans Nitroaromatic compounds Heteroaromatic compounds Carboxylic acid esters Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Organic oxoazanium compounds Monocarboxylic acids and derivatives Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organic zwitterions Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteromonocyclic compounds Substituents Furoic acid ester - Nitroaromatic compound - 2-nitrofuran - Heteroaromatic compound - Carboxylic acid ester - C-nitro compound - Organic nitro compound - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Organic oxoazanium - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Oxacycle - Organooxygen compound - Organonitrogen compound - Organic zwitterion - Organic oxygen compound - Organopnictogen compound - Organic oxide - Organic nitrogen compound - Hydrocarbon derivative - Aromatic heteromonocyclic compound Descripción This compound belongs to the class of organic compounds known as furoic acid esters. These are ester derivatives of furoic acid. External Descriptors Not available Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Estructura 3D Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Punto de fusión (°C) 98-101℃ Peso molecular 185.130 g/mol XLogP3 1.700 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 3 Exact Mass 185.032 Da Monoisotopic Mass 185.032 Da Topological Polar Surface Area 85.300 Ų Heavy Atom Count 13 Formal Charge 0 Complexity 211.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
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