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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Ester pentafluorofenílico de fmoc-L-prolina - ≥96% , CAS No.86060-90-4
Synonyms
Fmoc-Pro-OPfp, >=96.0% | MFCD00065672 | Fmoc-L-Pro-OPfp | N-alpha-(9-Fluorenylmethyloxycarbonyl)-L-proline pentafluorphenyl ester | F11064 | Fmoc-Pro-OPfp | 1,2-Pyrrolidinedicarboxylicacid,1-(9H-fluoren-9-ylmethyl)2-(pentafluorophenyl)ester,(2S)- | N-(9-F
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Why this grade ≥96% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Conservar a 2-8°C Ships Hielo húmedo Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Sinónimos
Fmoc-Pro-OPfp, >=96.0% | MFCD00065672 | Fmoc-L-Pro-OPfp | N-alpha-(9-Fluorenylmethyloxycarbonyl)-L-proline pentafluorphenyl ester | F11064 | Fmoc-Pro-OPfp | 1, 2-Pyrrolidinedicarboxylicacid, 1-(9H-fluoren-9-ylmethyl)2-(pentafluorophenyl)ester, (2S)- | N-(9-F
Especificaciones y pureza
≥96%
Condiciones de almacenamiento de almacenamiento
Conservar a 2-8°C
Nombres e identificadores Pubchem Sid 488192400 Sonrisas canónicas C1CC(N(C1)C(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24)C(=O)OC5=C(C(=C(C(=C5F)F)F)F)F IUPAC Name 1-O-(9H-fluoren-9-ylmethyl) 2-O-(2,3,4,5,6-pentafluorophenyl) (2S)-pyrrolidine-1,2-dicarboxylate InChIKey CQBLOHXKGUNWRV-SFHVURJKSA-N INCHI 1S/C26H18F5NO4/c27-19-20(28)22(30)24(23(31)21(19)29)36-25(33)18-10-5-11-32(18)26(34)35-12-17-15-8-3-1-6-13(15)14-7-2-4-9-16(14)17/h1-4,6-9,17-18H,5,10-12H2/t18-/m0/s1 Isómeros SMILES C1C[C@H](N(C1)C(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24)C(=O)OC5=C(C(=C(C(=C5F)F)F)F)F WGK Alemania 3 PubChem CID 2733412 Peso molecular 503.42 Beilstein 4731096
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Benzenoids Clase Fluorenes Subclass Not available Intermediate Tree Nodes Not available Direct Parent Fluorenes Alternative Parents Proline and derivatives Alpha amino acid esters Phenol esters Pyrrolidine carboxylic acids Phenoxy compounds Fluorobenzenes Aryl fluorides Carbamate esters Organic carbonic acids and derivatives Carboxylic acid esters Azacyclic compounds Monocarboxylic acids and derivatives Hydrocarbon derivatives Carbonyl compounds Organic oxides Organofluorides Organonitrogen compounds Organopnictogen compounds Molecular Framework Aromatic heteropolycyclic compounds Substituents Alpha-amino acid ester - Fluorene - Proline or derivatives - Phenol ester - Alpha-amino acid or derivatives - Phenoxy compound - Pyrrolidine carboxylic acid - Pyrrolidine carboxylic acid or derivatives - Fluorobenzene - Halobenzene - Aryl fluoride - Monocyclic benzene moiety - Aryl halide - Carbamic acid ester - Pyrrolidine - Carbonic acid derivative - Carboxylic acid ester - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Organooxygen compound - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Organopnictogen compound - Organofluoride - Organohalogen compound - Aromatic heteropolycyclic compound Descripción This compound belongs to the class of organic compounds known as fluorenes. These are compounds containing a fluorene moiety, which consists of two benzene rings connected through either a cyclopentane, cyclopentene, or cyclopenta-1,3-diene. 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) 127 - 129 °C Peso molecular 503.400 g/mol XLogP3 5.700 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 9 Rotatable Bond Count 6 Exact Mass 503.116 Da Monoisotopic Mass 503.116 Da Topological Polar Surface Area 55.800 Ų Heavy Atom Count 36 Formal Charge 0 Complexity 781.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 1 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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