Dicyclohexano-18-crown-6 - ≥98% , CAS No.16069-36-6

CAS: 16069-36-6 Cat. No.: D119931 Formula: C₂₀H₃₆O₆ Peso molecolare: 372.5 Beilstein Registry Number: 1130529 Numero EC: 240-216-4

GRADE & PURITY ≥98%

Synonyms

L-Cefamandole | AI3-62377 | Icosahydrodibenzo[b,k][1,4,7,10,13,16]hexaoxacyclooctadecine # | .beta.-Artemether | AKOS016344456 | 2,5,8,15,18,21-Hexaoxatricyclo(20.4.0.09,14)hexacosane | Crown ether dicyclohexyl-18-crown-6 | Ketocanazole | MFCD00005099 | A

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Panoramica

Anion activator,and complexing agent which solubilizes alkali metal ions in non-polar solvents.

Specifications

Sinonimi

L-Cefamandole | AI3-62377 | Icosahydrodibenzo[b,k][1,4,7,10,13,16]hexaoxacyclooctadecine # | .beta.-Artemether | AKOS016344456 | 2,5,8,15,18,21-Hexaoxatricyclo(20.4.0.09,14)hexacosane | Crown ether dicyclohexyl-18-crown-6 | Ketocanazole | MFCD00005099 | A

Specifiche e purezza

≥98%

Condizioni di conservazione di stoccaggio

Store at 2-8°C,Argon charged

Spedito in

Wet ice

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Purezza

≥98%

Nomi e identificatori

• Pubchem Sid: 508812195
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/508812195
• Sorrisi canonici: C1CCC2C(C1)OCCOCCOC3CCCCC3OCCOCCO2
• IUPAC Name: 2,5,8,15,18,21-hexaoxatricyclo[20.4.0.09,14]hexacosane
• InChIKey: BBGKDYHZQOSNMU-UHFFFAOYSA-N
• INCHI: 1S/C20H36O6/c1-2-6-18-17(5-1)23-13-9-21-11-15-25-19-7-3-4-8-20(19)26-16-12-22-10-14-24-18/h17-20H,1-16H2
• Isomeri SMILES: C1CCC2C(C1)OCCOCCOC3CCCCC3OCCOCCO2
• WGK Germania: 3
• RTECS: HP5385000
• Peso molecolare: 372.5
• Beilstein: 1130529
• Reaxy-Rn: 1130529
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1130529&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Classe: Organooxygen compounds
• Subclass: Ethers
• Intermediate Tree Nodes: Not available
• Direct Parent: Dialkyl ethers
• Alternative Parents: Oxacyclic compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteropolycyclic compounds
• Substituents: Oxacycle - Organoheterocyclic compound - Dialkyl ether - Hydrocarbon derivative - Aliphatic heteropolycyclic compound
• Descrizione: 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: 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.

DOI: 10.1186/s13321-016-0174-y

Obiettivi associati (umani)

MCF7 (126967 Activities)

Explore this target

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

MIA PaCa-2 (5949 Activities)

Explore this target

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

NCI-H460 (60772 Activities)

Explore this target

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

HeLa (62764 Activities)

Explore this target

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

Obiettivi associati (non umani)

Ttr Transthyretin (14 Activities)

Discover Target: Ttr

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

Escherichia coli (133304 Activities)

Explore this target

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

Bacillus subtilis (32866 Activities)

Explore this target

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

Gallus gallus (1187 Activities)

Explore this target

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 Toluene. Slightly soluble (13g/L, 26°C) in water.
• Sensibilità: Air Sensitive &Moisture sensitive.
• Punto di infiammabilità (°F): 230°F
• Punto di infiammabilità (°C): >110 °C
• Punto di ebollizione (°C): 344°C
• Punto di fusione (°C): 46-53℃
• Peso molecolare: 372.500 g/mol
• XLogP3: 1.800
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 0
• Exact Mass: 372.251 Da
• Monoisotopic Mass: 372.251 Da
• Topological Polar Surface Area: 55.400 Ų
• Heavy Atom Count: 26
• Formal Charge: 0
• Complexity: 300.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 4
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Riferimenti

1. Lianxiong Guan, Huiting Kang, Wei Liu, Dating Tian.  (2021)  Adsorption behavior of copper ions using crown ether-modified konjac glucomannan.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:33610605] [10.1016/j.ijbiomac.2021.02.129]

2. Yutong Hua, Junjie Liu, Deyi Zhang, Jintao Deng, Chang Liu, Xianhao Zhang, Zhiwei Zhu, Huan Wang, Yuanhua Shao.  (2024)  Electrochemical Behaviors of Ultramicro Triangular Pipettes.  ANALYTICAL CHEMISTRY,      [PMID:39694691] [10.1021/acs.analchem.4c04197]