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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Boc-L-Asp(OBzl)-OH - ≥98% , CAS No.7536-58-5
Synonyms
L-Aspartic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 4-(phenylmethyl) ester | (s)-4-(benzyloxy)-2-(tert-butoxycarbonylamino)-4-oxobutanoic acid | Boc-Asp(OBzl)-OH, >=99.0% (sum of enantiomers, HPLC) | DTXSID40884402 | Boc-Asp-(OBzl)-OH | Boc-Asp(OBzl)-OH |
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships Normal 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
L-Aspartic acid, N-[(1, 1-dimethylethoxy)carbonyl]-, 4-(phenylmethyl) ester | (s)-4-(benzyloxy)-2-(tert-butoxycarbonylamino)-4-oxobutanoic acid | Boc-Asp(OBzl)-OH, >=99.0% (sum of enantiomers, HPLC) | DTXSID40884402 | Boc-Asp-(OBzl)-OH | Boc-Asp(OBzl)-OH |
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Room temperature
Nombres e identificadores Pubchem Sid 488191972 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488191972 Sonrisas canónicas CC(C)(C)OC(=O)NC(CC(=O)OCC1=CC=CC=C1)C(=O)O IUPAC Name (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-oxo-4-phenylmethoxybutanoic acid InChIKey SOHLZANWVLCPHK-LBPRGKRZSA-N INCHI 1S/C16H21NO6/c1-16(2,3)23-15(21)17-12(14(19)20)9-13(18)22-10-11-7-5-4-6-8-11/h4-8,12H,9-10H2,1-3H3,(H,17,21)(H,19,20)/t12-/m0/s1 Isómeros SMILES CC(C)(C)OC(=O)N[C@@H](CC(=O)OCC1=CC=CC=C1)C(=O)O WGK Alemania 3 Peso molecular 323.34 Beilstein 2064127 Reaxy-Rn 2226328 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2226328&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 Aspartic acid and derivatives Alternative Parents Benzyloxycarbonyls Fatty acid esters Dicarboxylic acids and derivatives Carbamate esters Organic carbonic acids and derivatives Carboxylic acid esters Carboxylic acids Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic homomonocyclic compounds Substituents Aspartic acid or derivatives - Benzyloxycarbonyl - Fatty acid ester - Monocyclic benzene moiety - Dicarboxylic acid or derivatives - Fatty acyl - Benzenoid - Carbamic acid ester - Carboxylic acid ester - Carbonic acid derivative - Carboxylic acid - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Aromatic homomonocyclic compound Descripción This compound belongs to the class of organic compounds known as aspartic acid and derivatives. These are compounds containing an aspartic acid or a derivative thereof resulting from reaction of aspartic acid 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 Rotación específica [α] -20 ° (C=2, DMF) Punto de fusión (°C) 98-102°C Peso molecular 323.340 g/mol XLogP3 1.900 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 9 Exact Mass 323.137 Da Monoisotopic Mass 323.137 Da Topological Polar Surface Area 102.000 Ų Heavy Atom Count 23 Formal Charge 0 Complexity 423.000 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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