1-Ethylpiperidine - ≥98% , CAS No.766-09-6

CAS: 766-09-6 Cat. No.: E110307 Peso molecular: 113.2 Beilstein Registry Number: 102643 Número EC: 212-161-6

GRADE & PURITY ≥98%

Synonyms

N-ETHYLPIPERIDINE | NSC 2090 | MFCD00006507 | 1-Ethylpiperidine | 1-ethyl-piperidine | AMY23165 | EINECS 212-161-6 | InChI=1/C7H15N/c1-2-8-6-4-3-5-7-8/h2-7H2,1H | Q22829159 | 1-Ethylpiperidine, 99% | UNII-7IE43L0926 | N-Ethyl piperidine | NSC2090 | NSC-20

Storage

Room temperature,Argon charged

Shipped In

FedEx DG Service

Descripción general

Reactant for: Synthesis of multiprotected kanosamine Selective acylation in peptide synthesis Reagent for: Stereoselective aldol condensation reactions for synthesis of β-lactam antibiotics Diastereoselective synthesis of aldols Crossed Claisen ester condensation

Specifications

Sinónimos

N-ETHYLPIPERIDINE | NSC 2090 | MFCD00006507 | 1-Ethylpiperidine | 1-ethyl-piperidine | AMY23165 | EINECS 212-161-6 | InChI=1/C7H15N/c1-2-8-6-4-3-5-7-8/h2-7H2,1H | Q22829159 | 1-Ethylpiperidine, 99% | UNII-7IE43L0926 | N-Ethyl piperidine | NSC2090 | NSC-20

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Room temperature,Argon charged

Enviado en

FedEx DG Service

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 488181766
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488181766
• Sonrisas canónicas: CCN1CCCCC1
• IUPAC Name: 1-ethylpiperidine
• InChIKey: HTLZVHNRZJPSMI-UHFFFAOYSA-N
• INCHI: 1S/C7H15N/c1-2-8-6-4-3-5-7-8/h2-7H2,1H3
• Isómeros SMILES: CCN1CCCCC1
• WGK Alemania: 1
• RTECS: TN0250000
• Número ONU: 2386
• Grupo de embalaje: II
• Peso molecular: 113.2
• Beilstein: 102643
• Reaxy-Rn: 102643
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=102643&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Piperidines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Piperidines
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Piperidines
• Alternative Parents: Trialkylamines Azacyclic compounds Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Piperidine - Tertiary aliphatic amine - Tertiary amine - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Amine - Aliphatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as piperidines. These are compounds containing a piperidine ring, which is a saturated aliphatic six-member ring with one nitrogen atom and five carbon atoms.
• External Descriptors: piperidines

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.

DOI: 10.1186/s13321-016-0174-y

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: 1-ethylpiperidine salt of benzylpenicillin is considerably less soluble in amyl acetate and acetone.
• Sensibilidad: air sensitive
• Índice de refracción: 1.444
• Punto de inflamación (°F): 62.6 °F
• Punto de inflamación (°C): 17 °C
• Punto de ebullición (°C): 131°C
• Peso molecular: 113.200 g/mol
• XLogP3: 2.000
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 113.12 Da
• Monoisotopic Mass: 113.12 Da
• Topological Polar Surface Area: 3.200 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 55.400
• 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

Referencias

1. Yunfei Yang, Yixin Xu, Niya Ye, Dengji Zhang, Jingshuai Yang, Ronghuan He.  (2018)  Alkali Resistant Anion Exchange Membranes Based on Saturated Heterocyclic Quaternary Ammonium Cations Functionalized Poly(2,6-dimethyl-1,4-phenylene oxide)s.  JOURNAL OF THE ELECTROCHEMICAL SOCIETY,  165  (5): (F350).  [PMID:] [10.1149/2.1031805jes]