ε-Caprolactone - ≥97% , CAS No.502-44-3

CAS: 502-44-3 Cat. No.: C398060 Formula: C₆H₁₀O₂ Peso molecolare: 114.14 Beilstein Registry Number: 106919 Numero EC: 207-938-1

QUALITÀ & PUREZZA ≥97%

Synonyms

oxepan-2-one|Epsilon-caprolactone|CAPROLACTONE|6-Hexanolactone|502-44-3|2-Oxepanone|Hexan-6-olide|hexano-6-lactone|6-Hexanolide|1-Oxa-2-oxocycloheptane|1,6-Hexanolide|E-Caprolactone|Placcel M|epsilon-Caprolactone monomer|2-Oxacycloheptanone|24980-41-4|6-H

Storage

Room temperature,Desiccated

Shipped In

Normal

Specifiche

Sinonimi

oxepan-2-one | Epsilon-caprolactone | CAPROLACTONE | 6-Hexanolactone | 502-44-3 | 2-Oxepanone | Hexan-6-olide | hexano-6-lactone | 6-Hexanolide | 1-Oxa-2-oxocycloheptane | 1,6-Hexanolide | E-Caprolactone | Placcel M | epsilon-Caprolactone monomer | 2-Oxacycloheptanone | 24980-41-4 | 6-H

Specifiche e purezza

≥97%

Condizioni di conservazione di stoccaggio

Room temperature,Desiccated

Spedito in

Normal

Purezza

≥97%

Nomi e identificatori

Pubchem Sid

508811330

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508811330

Sorrisi canonici

C1CCC(=O)OCC1

IUPAC Name

oxepan-2-one

InChIKey

PAPBSGBWRJIAAV-UHFFFAOYSA-N

INCHI

1S/C6H10O2/c7-6-4-2-1-3-5-8-6/h1-5H2

Isomeri SMILES

C1CCC(=O)OCC1

WGK Germania

2

RTECS

MO8400000

Peso molecolare

114.14

Beilstein

106919

Reaxy-Rn

106919

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=106919&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Classe Lactones

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: Lactones
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Lactones
• Alternative Parents: Oxepanes Carboxylic acid esters Oxacyclic compounds Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Caprolactone - Oxepane - Lactone - Carboxylic acid ester - Oxacycle - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic heteromonocyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as lactones. These are cyclic esters of hydroxy carboxylic acids, containing a 1-oxacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring.
• External Descriptors: a small molecule

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

Obiettivi associati (umani)

PON1 Tbio Serum paraoxonase/arylesterase 1 (96 Activities)

Discover Target: PON1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Soluble in water (>1 mg/ml at 20 °C), ethanol, acetone, and diethyl ether.
• Indice di rifrazione: 1.462-1.464
• Punto di infiammabilità (°F): 228.2 °F
• Punto di infiammabilità (°C): 109℃
• Punto di ebollizione (°C): 140 °C/35 mmHg
• Punto di fusione (°C): -1°C
• Peso molecolare: 114.140 g/mol
• XLogP3: 0.000
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 114.068 Da
• Monoisotopic Mass: 114.068 Da
• Topological Polar Surface Area: 26.300 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 88.500
• 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