2,2,2-Trifluorethanol - für die Molekularbiologie, ≥99,8% , CAS No.75-89-8

CAS: 75-89-8 Cat. No.: T109511 Summenformel: C₂H₃F₃O Molekulargewicht: 100.04 Beilstein Registry Number: 1733203 EG-Nummer: 200-913-6 PubChem CID: 6409

QUALITÄT & REINHEIT Suitable for molecular biology, ≥99.8%

Synonyms

Trifluoroethanol|trifluroethanol|2,2,2-Trifluoroethanol redistilled from glass grade|beta, beta, beta-trifluoroethanol|2,2,2-Trifluoroethanol, NMR grade|2.2,2-trifluoroethanol|.beta.,.beta.,.beta.-Trifluoroethyl alcohol|2,2,-trifluoroethanol|trifluoro ethanol|beta,beta,beta-Trifluoroethyl alcohol|Trifluoroethanol;Ethanol, 2,2,2-trifluoro-;Trifluoroethyl alcohol|2,2,2-trifluoroethanole|2,2-Trifluoroethyl alcohol|BETA,BETA,BETA-TRIFLUOROETHANOL|Trifluoroethyl alcohol|2,2-Trifluoroethanol|TFE|ETHANOL,2,2,2-TRIFLUORO|2,2,2-trifluoro ethanol|2,2,2-Trifluoroethan-1-Ol|Perfluoro-1,1-dihydroethanol|Ethanol, 2,2,2-trifluoro-|2,2,2trifluoroethanol|2,2,2-TRIFLUOROETHANOL|2,2,2-tri-fluoroethanol|2,2,2-trifluoro-ethanol|trifluoroethylalcohol|2,2,2-trifluoroethylalcohol|ETF|2,2,2,-trifluoroethanol|2,2,2-trifluoroetanol|tfetoh|2.2.2-trifluoroethanol|2,2,2 trifluoroethanol|2,2,2 trifluoro-ethanol|2,2,2-trifloro ethanol|2,2,2-TRIFLUORETHANOL|1,1,1-Trifluoro-2-ethanol|2,2,2-trifluroethanol|2,2,2-Trifluoroethyl alcohol|trifluorethanol|TRIFLUOROETHANOL [MI]

Storage

Raumtemperatur

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Übersicht

2,2,2-Trifluoroethanol (TFE) is an organic compound with the chemical formula CF3CH2OH. TFE is a commonly used solvent in organic synthesis. It can also be used as a cosolvent in the experimental study of proteins and peptides.
Application
2,2,2-Trifluoroethanol can be used as a solvent:
In the synthesis of 2-amino-3-cyano-4H-chromene and tetrahydrobenzo[b]pyran derivatives by catalyst free one-pot condensation of aldehydes, malononitrile and resorcinol or dimedone.
In the N-formylation of amines with formic acid in the presence of heterogeneous ZIF-8 (zeolitic imidazolate framework) catalyst.
In the preparation of 2-substituted-2,3-dihydro-4(1H)-quinazolinone derivatives by condensation of anthranilamide with alkyl, aryl, or heteroaryl ketones or aldehydes.
In the mild and selective oxidation of sulfur compounds using H2O2(hydrogen peroxide).

Spezifikationen

Synonyme

Trifluoroethanol | trifluroethanol | 2,2,2-Trifluoroethanol redistilled from glass grade | beta, beta, beta-trifluoroethanol | 2,2,2-Trifluoroethanol, NMR grade | 2.2,2-trifluoroethanol | .beta.,.beta.,.beta.-Trifluoroethyl alcohol | 2,2,-trifluoroethanol | trifluoro ethanol | beta,beta,beta-Trifluoroethyl alcohol | Trifluoroethanol;Ethan Show more

Spezifikationen & Reinheit

für die Molekularbiologie, ≥99,8%

Storage

Raumtemperatur

Verschickt in

FedEx DG Service

Note

Suitable for molecular biology

Reinheit

≥99.8%

Namen und Kennungen

Kanonisches Lächeln

C(C(F)(F)F)O

IUPAC Name

2,2,2-trifluoroethanol

InChIKey

RHQDFWAXVIIEBN-UHFFFAOYSA-N

INCHI

1S/C2H3F3O/c3-2(4,5)1-6/h6H,1H2

Isomere SMILES

C(C(F)(F)F)O

WGK Deutschland

1

RTECS

KM5250000

PubChem CID

6409

UN-Nummer

1986

Verpackungsgruppe

III

Molekulargewicht

100.04

Beilstein

1733203

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organohalogen compounds
    • Klasse Halohydrins
      • Subclass Fluorohydrins

• Kingdom: Organic compounds
• Superclass: Organohalogen compounds
• Klasse: Halohydrins
• Subclass: Fluorohydrins
• Intermediate Tree Nodes: Not available
• Direct Parent: Fluorohydrins
• Alternative Parents: Primary alcohols Organofluorides Hydrocarbon derivatives Alkyl fluorides
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Fluorohydrin - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Organofluoride - Alkyl halide - Alkyl fluoride - Alcohol - Aliphatic acyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as fluorohydrins. These are alcohols substituted by a fluorine atom at a saturated carbon atom otherwise bearing only hydrogen or hydrocarbyl groups.
• External Descriptors: fluoroalcohol

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

Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Empfindlichkeit: Moisture sensitive
• Brechungsindex: 1.2907
• Flammpunkt (°F): 84°F
• Flammpunkt (°C): 29℃
• Siedepunkt (°C): 77-80°C
• Schmelzpunkt (°C): -45°C
• Molekulargewicht: 100.040 g/mol
• XLogP3: 0.400
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 0
• Exact Mass: 100.014 Da
• Monoisotopic Mass: 100.014 Da
• Topological Polar Surface Area: 20.200 Ų
• Heavy Atom Count: 6
• Formal Charge: 0
• Complexity: 38.500
• 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