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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Ethyl N-Boc-piperidine-4-carboxylate - ≥97% , CAS No.142851-03-4
Synonyms
1-(tert-butyl) 4-ethyl tetrahydro-1,4(2h)-pyridinedicarboxylate | 1-Boc-piperidine-4-carboxylicacidethylester | STL185663 | 1-Boc-4-piperidinecarboxylic Acid Ethyl Ester | Ethyl 1-(tert-butoxycarbonyl)-4-piperidinecarboxylate | Ethyl N-Boc-piperidine-4-ca
Storage
Store at 2-8°C,Argon charged
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Why this grade ≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at 2-8°C,Argon charged 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.
Descripción general Usually used in a palladium-catalyzed α-arylation of esters with heterocyclic bromides and chlorides; which can lead to 4-pyridylpiperidinyl esters.
Specifications Sinónimos
1-(tert-butyl) 4-ethyl tetrahydro-1, 4(2h)-pyridinedicarboxylate | 1-Boc-piperidine-4-carboxylicacidethylester | STL185663 | 1-Boc-4-piperidinecarboxylic Acid Ethyl Ester | Ethyl 1-(tert-butoxycarbonyl)-4-piperidinecarboxylate | Ethyl N-Boc-piperidine-4-ca
Especificaciones y pureza
≥97%
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C, Argon charged
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores Pubchem Sid 504761539 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504761539 Sonrisas canónicas CCOC(=O)C1CCN(CC1)C(=O)OC(C)(C)C IUPAC Name 1-O-tert-butyl 4-O-ethyl piperidine-1,4-dicarboxylate InChIKey MYHJCTUTPIKNAT-UHFFFAOYSA-N INCHI 1S/C13H23NO4/c1-5-17-11(15)10-6-8-14(9-7-10)12(16)18-13(2,3)4/h10H,5-9H2,1-4H3 Isómeros SMILES CCOC(=O)C1CCN(CC1)C(=O)OC(C)(C)C WGK Alemania 3 Peso molecular 257.33 Reaxy-Rn 6601553 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=6601553&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 Organoheterocyclic compounds Clase Piperidines Subclass Piperidinecarboxylic acids and derivatives Intermediate Tree Nodes Not available Direct Parent Piperidinecarboxylic acids Alternative Parents Carbamate esters Organic carbonic acids and derivatives Carboxylic acid esters Monocarboxylic acids and derivatives Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aliphatic heteromonocyclic compounds Substituents Piperidinecarboxylic acid - Carbamic acid ester - Carboxylic acid ester - Carbonic acid derivative - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Azacycle - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Carbonyl group - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Aliphatic heteromonocyclic compound Descripción This compound belongs to the class of organic compounds known as piperidinecarboxylic acids. These are compounds containing a piperidine ring which bears a carboxylic acid group. 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 Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Solubilidad Soluble in CHCI3: 25 mg/ml Sensibilidad Hygroscopic,Heat Sensitive Índice de refracción 1.46 Punto de inflamación (°F) >230 °F Punto de inflamación (°C) >110 °C Punto de ebullición (°C) 140 °C/0.098 mmHg Peso molecular 257.329 g/mol XLogP3 1.800 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 5 Exact Mass 257.163 Da Monoisotopic Mass 257.163 Da Topological Polar Surface Area 55.800 Ų Heavy Atom Count 18 Formal Charge 0 Complexity 301.000 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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