Cas no 758-48-5 (Ethanamine,1,1,2,2,2-pentafluoro-N-(1,1,2,2,2-pentafluoroethyl)-N-(trifluoromethyl)-)

Ethanamine,1,1,2,2,2-pentafluoro-N-(1,1,2,2,2-pentafluoroethyl)-N-(trifluoromethyl)- structure
758-48-5 structure
Product Name:Ethanamine,1,1,2,2,2-pentafluoro-N-(1,1,2,2,2-pentafluoroethyl)-N-(trifluoromethyl)-
CAS No:758-48-5
MF:C5F13N
MW:321.03944683075
CID:571736
PubChem ID:136571
Update Time:2025-07-09

Ethanamine,1,1,2,2,2-pentafluoro-N-(1,1,2,2,2-pentafluoroethyl)-N-(trifluoromethyl)- Chemical and Physical Properties

Names and Identifiers

    • Ethanamine,1,1,2,2,2-pentafluoro-N-(1,1,2,2,2-pentafluoroethyl)-N-(trifluoromethyl)-
    • Ethanamine, 1,?1,?2,?2,?2-?pentafluoro-?N-?(1,?1,?2,?2,?2-?pentafluoroethyl)?-?N-?(trifluoromethyl)?-
    • Perfluor-N-methyl-N,N-diethylamine
    • 1,1,2,2,2-Pentafluoro-N-(pentafluoroethyl)-N-(trifluoromethyl)ethanamine
    • 758-48-5
    • 1,1,2,2,2-pentafluoro-N-(1,1,2,2,2-pentafluoroethyl)-N-(trifluoromethyl)ethanamine
    • Perfluoro(diethylmethylamine)
    • SCHEMBL7628609
    • Perfluoromethyldiethylamine
    • ETHANAMINE, 1,1,2,2,2-PENTAFLUORO-N-(1,1,2,2,2-PENTAFLUOROETHYL)-N-(TRIFLUOROMETHYL)-
    • DIETHYLAMINE, 1,1,1,1,2,2,2,2,2,2-DECAFLUORO-N-(TRIFLUOROMETHYL)-
    • N-(trifluoro-methyl)bis(penta-fluoroethyl) amine
    • AKOS037621746
    • MD-46
    • UNII-QZ8LSG9H5L
    • QZ8LSG9H5L
    • perfluorodiethyl-methylamine
    • TRIFLUOROMETHYLBIS(PENTAFLUOROETHYL)AMINE
    • ETHANAMINE, 1,1,2,2,2-PENTAFLUORO-N-(PENTAFLUOROETHYL)-N-(TRIFLUOROMETHYL)-
    • KMPITNDOTGKQSE-UHFFFAOYSA-N
    • Q7168160
    • DTXSID10226714
    • BIS(PENTAFLUOROETHYL)(TRIFLUOROMETHYL)AMINE
    • Inchi: 1S/C5F13N/c6-1(7,8)3(12,13)19(5(16,17)18)4(14,15)2(9,10)11
    • InChI Key: KMPITNDOTGKQSE-UHFFFAOYSA-N
    • SMILES: FC(C(F)(F)F)(N(C(F)(F)F)C(C(F)(F)F)(F)F)F

Computed Properties

  • Exact Mass: 320.9823
  • Monoisotopic Mass: 320.9823151g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 14
  • Heavy Atom Count: 19
  • Rotatable Bond Count: 2
  • Complexity: 291
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 5.2
  • Topological Polar Surface Area: 3.2?2

Experimental Properties

  • Boiling Point: 46.44°C (rough estimate)
  • PSA: 3.24

Ethanamine,1,1,2,2,2-pentafluoro-N-(1,1,2,2,2-pentafluoroethyl)-N-(trifluoromethyl)- Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
SHANG HAI HAO HONG Biomedical Technology Co., Ltd.
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Perfluoro(diethylmethylamine)
758-48-5 98%
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¥2730.00 2024-07-28
SHANG HAI HAO HONG Biomedical Technology Co., Ltd.
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Additional information on Ethanamine,1,1,2,2,2-pentafluoro-N-(1,1,2,2,2-pentafluoroethyl)-N-(trifluoromethyl)-

Introduction to Ethanamine, 1,1,2,2,2-Pentafluoro-N-(1,1,2,2,2-Pentafluoroethyl)-N-(Trifluoromethyl)

Ethanamine is a fundamental organic compound with a wide range of applications in various industries. The compound Ethanamine, 1,1,2,2,2-pentafluoro-N-(1,1,2,2,2-pentafluoroethyl)-N-(trifluoromethyl) (CAS No. 758-48-5) is a highly fluorinated derivative of ethanamine. This compound has garnered significant attention due to its unique chemical properties and potential applications in fields such as materials science and pharmaceuticals.

The structure of Ethanamine is characterized by its two-carbon chain with an amine functional group. The addition of multiple fluorine atoms in the case of Ethanamine, 1,1,2,2,2-pentafluoro-N-(1,1,2,2,pentafluoroethyl)-N-(trifluoromethyl) significantly alters its chemical behavior. Fluorination is known to enhance stability and reactivity in many organic compounds. Recent studies have highlighted the potential of this compound as a building block for advanced materials and as a catalyst in organic synthesis.

One of the most promising applications of this compound lies in its role as an intermediate in the synthesis of fluoropolymers. These polymers are widely used in industries such as aerospace and electronics due to their exceptional thermal and chemical resistance. The high fluorination level in Ethanamine derivatives makes them ideal candidates for such applications.

Furthermore, research has shown that Ethanamine derivatives can be used as precursors for the synthesis of novel pharmaceutical agents. The trifluoromethyl group present in this compound contributes to its lipophilicity and bioavailability. This makes it a valuable molecule in drug design and development.

In terms of environmental impact and safety considerations,Ethanamine derivatives are generally considered stable under normal conditions. However,special precautions should be taken during handling due to their chemical reactivity.

Recent advancements in computational chemistry have enabled researchers to better understand the electronic structure and reactivity patterns of Ethanamine derivatives. These insights are paving the way for new synthetic routes and applications.

In conclusion,Ethanamine, CAS No.758-48-5 represents a versatile molecule with significant potential across multiple disciplines.The combination of its unique chemical properties with cutting-edge research findings positions it as a key player in future technological advancements.

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