15-Krone-5 - ≥97% , CAS No.33100-27-5

CAS: 33100-27-5 Cat. No.: C105798 Summenformel: C₁₀H₂₀O₅ Molekulargewicht: 220.26 Beilstein Registry Number: 1618144 EG-Nummer: 251-379-6

QUALITÄT & REINHEIT ≥97%

Synonyms

15C5 | 15-Crown-5(1,4,7,10,13-Pentaoxacyclopentadecane) | EN300-6743610 | EYO | MFCD00005110 | 1, 4, 7, 10, 13-pentaoxacyclopentadecane | 15-Crown 5-Ether | 15-Crown-5, Vetec(TM) reagent grade, 98% | AKOS005622525 | 15-Crown-5, purum, >=98.0% (GC) | EINEC

Storage

Argon charged,Room temperature

Shipped In

Normal

Spezifikationen

Synonyme

15C5 | 15-Crown-5(1,4,7,10,13-Pentaoxacyclopentadecane) | EN300-6743610 | EYO | MFCD00005110 | 1, 4, 7, 10, 13-pentaoxacyclopentadecane | 15-Crown 5-Ether | 15-Crown-5, Vetec(TM) reagent grade, 98% | AKOS005622525 | 15-Crown-5, purum, >=98.0% (GC) | EINEC

Spezifikationen & Reinheit

≥97%

Storage

Argon charged,Room temperature

Verschickt in

Normal

Reinheit

≥97%

Namen und Kennungen

Pubchem Sid

488183275

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488183275

Kanonisches Lächeln

C1COCCOCCOCCOCCO1

IUPAC Name

1,4,7,10,13-pentaoxacyclopentadecane

InChIKey

VFTFKUDGYRBSAL-UHFFFAOYSA-N

INCHI

1S/C10H20O5/c1-2-12-5-6-14-9-10-15-8-7-13-4-3-11-1/h1-10H2

Isomere SMILES

C1COCCOCCOCCOCCO1

WGK Deutschland

3

RTECS

SB0200000

Molekulargewicht

220.26

Beilstein

1618144

Reaxy-Rn

1618144

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1618144&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Klasse: 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
• Beschreibung: 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

Zugehörige Ziele (nicht menschlich)

Ttr Transthyretin (14 Activities)

Discover Target: Ttr

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

Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Löslichkeit: Miscible with organic solvents.
• Empfindlichkeit: Moisture sensitive
• Brechungsindex: 1.465
• Flammpunkt (°F): 235.4 °F
• Flammpunkt (°C): 113 °C
• Siedepunkt (°C): 93-96 °C/0.05 mmHg
• Schmelzpunkt (°C): -20°C
• Molekulargewicht: 220.260 g/mol
• XLogP3: -0.500
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 0
• Exact Mass: 220.131 Da
• Monoisotopic Mass: 220.131 Da
• Topological Polar Surface Area: 46.200 Ų
• Heavy Atom Count: 15
• Formal Charge: 0
• Complexity: 86.200
• 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