12-Crown-4 - ≥98% , CAS No.294-93-9

CAS: 294-93-9 Cat. No.: C102036 Fórmula: C₈H₁₆O₄ Peso molecular: 176.21 Beilstein Registry Number: 1363064 Número EC: 206-036-5

GRADE & PURITY ≥98%

Synonyms

EOCT | 12-crown-4-ether | CCRIS 157 | D89315 | FT-0607231 | CHEBI:32399 | SCHEMBL236725 | 1,4,7,10-TETRAOXACYCLODODECANE | 1,4,7,10-tetraoxacyclo-dodecane | 1,4,7,10tetraoxa-Cyclododecane | K6069P2C2A | LS-13523 | MFCD00005103 | 5-19-11-00334 (Beilstein H

Storage

Store at 2-8°C

Shipped In

Wet ice

Descripción general

12-Crown-4 is a Phase transfer catalyst, complexing-agent for lithium. Aprotic "solvent" for alkali metals, the sodium solution is a strong reducing agent.
An aprotic "solvent" for alkali metals, the sodium solution is a strong reducing agent

Specifications

Sinónimos

EOCT | 12-crown-4-ether | CCRIS 157 | D89315 | FT-0607231 | CHEBI:32399 | SCHEMBL236725 | 1,4,7,10-TETRAOXACYCLODODECANE | 1,4,7,10-tetraoxacyclo-dodecane | 1,4,7,10tetraoxa-Cyclododecane | K6069P2C2A | LS-13523 | MFCD00005103 | 5-19-11-00334 (Beilstein H

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C

Enviado en

Wet ice

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥98%

Nombres e identificadores

Pubchem Sid

504751814

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504751814

Sonrisas canónicas

C1COCCOCCOCCO1

IUPAC Name

1,4,7,10-tetraoxacyclododecane

InChIKey

XQQZRZQVBFHBHL-UHFFFAOYSA-N

INCHI

1S/C8H16O4/c1-2-10-5-6-12-8-7-11-4-3-9-1/h1-8H2

Isómeros SMILES

C1COCCOCCOCCO1

WGK Alemania

3

RTECS

XF0550000

Número ONU

2810

Peso molecular

176.21

Beilstein

1363064

Reaxy-Rn

1363064

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1363064&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Clase Organooxygen compounds
      • Subclass Ethers

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Clase: Organooxygen compounds
• Subclass: Ethers
• Intermediate Tree Nodes: Not available
• Direct Parent: Dialkyl ethers
• Alternative Parents: Oxacyclic compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Oxacycle - Organoheterocyclic compound - Dialkyl ether - Hydrocarbon derivative - Aliphatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as dialkyl ethers. These are organic compounds containing the dialkyl ether functional group, with the formula ROR', where R and R' are alkyl groups.
• External Descriptors: saturated organic heteromonocyclic parent - crown ether

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: Fully miscible in water.
• Sensibilidad: Air sensitive.Light Sensitive
• Punto de congelación (°C): 17 °C
• Índice de refracción: 1.462-1.463
• Punto de inflamación (°F): 235.4 °F
• Punto de inflamación (°C): 113 °C
• Punto de ebullición (°C): 61-70°C/0.5mmHg
• Punto de fusión (°C): 16°C
• Peso molecular: 176.210 g/mol
• XLogP3: 0.000
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 0
• Exact Mass: 176.105 Da
• Monoisotopic Mass: 176.105 Da
• Topological Polar Surface Area: 36.900 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 65.099
• 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