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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items N-Phthaloyl-L-phenylalanine - ≥98% , CAS No.5123-55-7
Synonyms
F10912 | BB 0249704 | 2-(1,3-Dioxo-1,3-dihydro-2H-isoindol-2-yl)-3-phenylpropanoic acid # | NCGC00013262 | NCGC00096381-01 | AS-46920 | NSC 338600 | N-Pht-Phe-OH | 2-Isoindolineacetic acid,3-dioxo-, (S)-(-)- | (S)-N-Phthaloylphenylalanine | 2-Isoindolinea
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at 2-8°C Ships Wet ice 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
F10912 | BB 0249704 | 2-(1, 3-Dioxo-1, 3-dihydro-2H-isoindol-2-yl)-3-phenylpropanoic acid # | NCGC00013262 | NCGC00096381-01 | AS-46920 | NSC 338600 | N-Pht-Phe-OH | 2-Isoindolineacetic acid, 3-dioxo-, (S)-(-)- | (S)-N-Phthaloylphenylalanine | 2-Isoindolinea
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C
Enviado en
Wet ice
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Nombres e identificadores Pubchem Sid 504758504 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504758504 Sonrisas canónicas C1=CC=C(C=C1)CC(C(=O)O)N2C(=O)C3=CC=CC=C3C2=O IUPAC Name (2S)-2-(1,3-dioxoisoindol-2-yl)-3-phenylpropanoic acid InChIKey VAYRSTHMTWUHGE-AWEZNQCLSA-N INCHI 1S/C17H13NO4/c19-15-12-8-4-5-9-13(12)16(20)18(15)14(17(21)22)10-11-6-2-1-3-7-11/h1-9,14H,10H2,(H,21,22)/t14-/m0/s1 Isómeros SMILES C1=CC=C(C=C1)C[C@@H](C(=O)O)N2C(=O)C3=CC=CC=C3C2=O WGK Alemania 3 Peso molecular 295.29 Beilstein 90080 Reaxy-Rn 90078 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=90078&ln=
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 Organic acids and derivatives Clase Carboxylic acids and derivatives Subclass Amino acids, peptides, and analogues Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives Direct Parent Phenylalanine and derivatives Alternative Parents Phthalimides Phenylpropanoic acids Amphetamines and derivatives Isoindoles N-substituted carboxylic acid imides Monocarboxylic acids and derivatives Carboxylic acids Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic heteropolycyclic compounds Substituents Phenylalanine or derivatives - Phthalimide - 3-phenylpropanoic-acid - Amphetamine or derivatives - Isoindolone - Isoindoline - Isoindole - Isoindole or derivatives - Monocyclic benzene moiety - Benzenoid - Carboxylic acid imide, n-substituted - Carboxylic acid imide - Carboxylic acid - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Aromatic heteropolycyclic compound Descripción This compound belongs to the class of organic compounds known as phenylalanine and derivatives. These are compounds containing phenylalanine or a derivative thereof resulting from reaction of phenylalanine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. 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 Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Solubilidad Soluble in methanol. (almost transparency) Rotación específica [α] -216.5 ° (C=2, EtOH) Punto de fusión (°C) 181-185°C Peso molecular 295.290 g/mol XLogP3 2.500 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 4 Exact Mass 295.084 Da Monoisotopic Mass 295.084 Da Topological Polar Surface Area 74.700 Ų Heavy Atom Count 22 Formal Charge 0 Complexity 445.000 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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