Cas no 22560-21-0 (Potassium Triethylborohydride)

Potassium Triethylborohydride (KBEt?H) is a highly reactive reducing agent commonly used in organic synthesis. Its strong nucleophilic and basic properties make it particularly effective for the reduction of hindered ketones, esters, and epoxides, as well as for deprotonation reactions. The reagent offers superior selectivity and reactivity compared to traditional hydride reagents like lithium aluminum hydride (LiAlH?) or sodium borohydride (NaBH?). It is often employed in the preparation of organoboron compounds and as a catalyst in asymmetric synthesis. Due to its air- and moisture-sensitive nature, it is typically handled under inert conditions. Its versatility and efficiency make it a valuable tool in advanced synthetic chemistry applications.
Potassium Triethylborohydride structure
Potassium Triethylborohydride structure
Product Name:Potassium Triethylborohydride
CAS No:22560-21-0
MF:C6H15BK
MW:137.092602968216
MDL:MFCD00011702
CID:266060
PubChem ID:24852782
Update Time:2025-11-01

Potassium Triethylborohydride Chemical and Physical Properties

Names and Identifiers

    • Borate(1-),triethylhydro-, potassium (1:1), (T-4)-
    • Potassium triethylborohydride
    • Potassium triethylborohydride solution
    • Potassium triethylborohydride, 1.0 M solution in THF, SpcSeal
    • potassium,triethylboranuide
    • bottle
    • Potassium triethylborohydride, 1.0M in THF, in Sure
    • Potassium triethylborohydride, 1M solution in THF, AcroSeal
    • Seal&trade
    • SEAL? BOTTLE
    • Potassium hydrotriethylborate
    • Potassium triethylhydridoborate
    • Potassium triethylhydridoborate(1-)
    • Potassium triethylhydroborate(1-)
    • AKOS025294942
    • 22560-21-0
    • DTXSID50945210
    • Potassium triethyl(hydrido)borate(1-)
    • Potassium triethylborohydride, 1.0M in THF, in Sure/Seal TM bottle
    • MFCD00011702
    • J-014763
    • potassiumtriethylborohydride,calselect?kt,
    • potassiumtriethylborohydride,calselect?kt,intetrahydrofuran
    • potassium triethylhydroborate
    • Potassium triethylborohydride, in tetrahydrofuran, 1M solution
    • POTASSIUM TRIETHYLBOROHYDRIDE, 1.0M SOLU TION IN TETRAHYDROFURAN
    • Potassiumtriethylborohydride,1.0MinTHF,inSure/Sealbottle
    • Potassium Triethylborohydride
    • MDL: MFCD00011702
    • Inchi: 1S/C6H15B.K/c1-4-7(5-2)6-3;/h4-6H2,1-3H3;/q-1;+1
    • InChI Key: JSWZHFBULBZRJI-UHFFFAOYSA-N
    • SMILES: [K+].C([B-](CC)CC)C |^1:2|

Computed Properties

  • Exact Mass: 137.09000
  • Monoisotopic Mass: 137.0903871g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 8
  • Rotatable Bond Count: 3
  • Complexity: 30
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 0?2
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: nothing

Experimental Properties

  • Color/Form: Not available
  • Density: 0.902?g/mL?at 25?°C
  • Melting Point: No data available
  • Boiling Point: No data available
  • Flash Point: Fahrenheit: 1.4 ° f < br / > Celsius: -17 ° C < br / >
  • PSA: 0.00000
  • LogP: 2.54090
  • Solubility: Not available
  • Vapor Pressure: No data available
  • Sensitiveness: air sensitive, moisture sensitive
  • Color/Form: 1.0?M in THF

Potassium Triethylborohydride Security Information

Potassium Triethylborohydride Customs Data

  • HS CODE:29310099

Potassium Triethylborohydride Pricemore >>

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Potassium Triethylborohydride Related Literature

Additional information on Potassium Triethylborohydride

Introduction to Potassium Triethylborohydride (CAS No. 22560-21-0)

Potassium Triethylborohydride, a compound with the chemical formula K[BH(C?H?)?], is a significant reagent in the field of organic synthesis and pharmaceutical development. This compound, identified by its CAS number 22560-21-0, has garnered considerable attention due to its unique properties and versatile applications. As a hydride transfer agent, it plays a crucial role in various synthetic transformations, particularly in the reduction of unsaturated compounds and the synthesis of complex organic molecules.

The use of Potassium Triethylborohydride has been extensively explored in recent years, particularly in the context of drug discovery and development. Its ability to facilitate the reduction of ketones and aldehydes to their corresponding alcohols has made it an indispensable tool in medicinal chemistry. Recent studies have highlighted its application in the synthesis of biologically active compounds, where its selectivity and efficiency are highly valued.

One of the most compelling aspects of Potassium Triethylborohydride is its stability under various reaction conditions. Unlike some other hydride transfer agents, it remains stable in both aqueous and organic solvents, making it a versatile choice for a wide range of synthetic protocols. This stability is attributed to its potassium counterion and the bulky ethyl groups attached to the boron atom, which provide excellent solubility and reactivity.

In recent research, Potassium Triethylborohydride has been employed in the synthesis of complex pharmaceutical intermediates. For instance, it has been used to reduce sensitive functional groups without causing unwanted side reactions. This property is particularly valuable in industrial settings where high yields and purity are essential. Additionally, its compatibility with various catalysts has allowed for further optimization of synthetic routes, leading to more efficient production processes.

The compound's role in asymmetric synthesis has also been a subject of intense investigation. Researchers have leveraged its chiral auxiliary properties to achieve high enantiomeric excess in the synthesis of optically active compounds. These findings have significant implications for the development of chiral drugs, which are often required to exhibit specific biological activities depending on their stereochemistry.

Moreover, Potassium Triethylborohydride has found applications in the field of materials science. Its ability to participate in cross-coupling reactions has made it useful in the synthesis of advanced materials with tailored properties. For example, it has been used in the preparation of conductive polymers and nanomaterials, which have potential applications in electronics and energy storage devices.

The environmental impact of using Potassium Triethylborohydride has also been a focus of recent studies. Researchers have been working on developing greener synthetic methods that minimize waste and reduce energy consumption. Some studies have demonstrated that this compound can be effectively recycled, thereby reducing its environmental footprint. These efforts align with broader trends in sustainable chemistry aimed at minimizing the ecological impact of chemical processes.

Another area where Potassium Triethylborohydride has shown promise is in the field of biocatalysis. Its ability to interact with enzymes has led to novel approaches for catalyzing biochemical reactions under mild conditions. This has opened up new possibilities for biotechnological applications, where traditional chemical methods may be less effective or environmentally friendly.

In conclusion, Potassium Triethylborohydride (CAS No. 22560-21-0) is a multifaceted compound with a wide range of applications in organic synthesis, pharmaceutical development, materials science, and biocatalysis. Its unique properties as a hydride transfer agent make it an invaluable tool for researchers seeking efficient and selective synthetic methods. As our understanding of its capabilities continues to grow, so too will its importance in advancing chemical research and industrial applications.

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