Cas no 106356-53-0 (Borane,2-propen-1-ylbis[(1S,2R,3S,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-3-yl]-)

Borane,2-propen-1-ylbis[(1S,2R,3S,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-3-yl]- structure
106356-53-0 structure
Product Name:Borane,2-propen-1-ylbis[(1S,2R,3S,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-3-yl]-
CAS No:106356-53-0
MF:C23H39B
MW:326.366767168045
CID:133558
PubChem ID:24885431
Update Time:2025-07-17

Borane,2-propen-1-ylbis[(1S,2R,3S,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-3-yl]- Chemical and Physical Properties

Names and Identifiers

    • Borane,2-propen-1-ylbis[(1S,2R,3S,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-3-yl]-
    • (+)-Ipc2B(allyl)borane solution
    • (+)-(Ipc)2B(allyl)
    • (+)-allylB(Ipc)2
    • (+)-B-Allyldiisopinocampheylborane solution
    • (+)-Ipc2B(allyl)
    • (+)-Ipc2B(allyl)borane
    • (+)-Ipc2Ballyl
    • 678503_ALDRICH
    • CTK8E6888
    • (+)-Ipc2B(allyl) solution
    • (+)-IPC2B(ALLYL), 1M IN PENTANE
    • (+)-Ipc2B(allyl), 1M in dioxane
    • (+)-Ipc2B(allyl)borane solution 1 M in pentane
    • 106356-53-0
    • AKOS025294027
    • allylbis((1S,2R,3S,5S)-2,6,6-trimethylbicyclo[3.1.1]heptan-3-yl)borane
    • prop-2-enyl-bis[(1S,2R,3S,5S)-2,6,6-trimethyl-3-bicyclo[3.1.1]heptanyl]borane
    • ZIXZBDJFGUIKJS-AXSQLCHVSA-N
    • DTXSID00450243
    • J-001580
    • Inchi: 1S/C23H39B/c1-8-9-24(20-12-16-10-18(14(20)2)22(16,4)5)21-13-17-11-19(15(21)3)23(17,6)7/h8,14-21H,1,9-13H2,2-7H3/t14-,15-,16+,17+,18-,19-,20-,21-/m0/s1
    • InChI Key: ZIXZBDJFGUIKJS-AXSQLCHVSA-N
    • SMILES: [C@H]12C[C@H](C[C@H](B(CC=C)[C@H]3C[C@H]4C[C@@H]([C@@H]3C)C4(C)C)[C@H]1C)C2(C)C

Computed Properties

  • Exact Mass: 325.31827
  • Monoisotopic Mass: 326.3144814g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 0
  • Heavy Atom Count: 24
  • Rotatable Bond Count: 4
  • Complexity: 476
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 8
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 0?2

Experimental Properties

  • Density: 0.735?g/mL?at 25?°C
  • Boiling Point: 35-36?°C
  • Flash Point: Fahrenheit: -56.2 ° f
    Celsius: -49 ° c
  • PSA: 0
  • LogP: 6.81180
  • Color/Form: 1?M in pentane
  • Optical Activity: [α]20/D +14°, c =?1 in pentane

Borane,2-propen-1-ylbis[(1S,2R,3S,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-3-yl]- Security Information

Borane,2-propen-1-ylbis[(1S,2R,3S,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-3-yl]- Pricemore >>

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Borane,2-propen-1-ylbis[(1S,2R,3S,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-3-yl]- Related Literature

Additional information on Borane,2-propen-1-ylbis[(1S,2R,3S,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-3-yl]-

Recent Advances in the Study of Borane,2-propen-1-ylbis[(1S,2R,3S,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-3-yl]- (CAS: 106356-53-0)

Borane,2-propen-1-ylbis[(1S,2R,3S,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-3-yl]-, with the CAS number 106356-53-0, is a specialized borane compound that has garnered significant attention in the field of chemical biology and medicinal chemistry. This compound is characterized by its unique bicyclic structure and the presence of borane moieties, which make it a valuable candidate for various applications, including asymmetric synthesis, catalysis, and drug development. Recent studies have explored its potential in enhancing the efficiency of organic transformations and its role in the development of novel therapeutic agents.

The synthesis and characterization of Borane,2-propen-1-ylbis[(1S,2R,3S,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-3-yl]- have been the focus of several research efforts. A study published in the Journal of Organic Chemistry (2023) detailed a novel synthetic route that improves the yield and purity of this compound. The researchers employed advanced spectroscopic techniques, including NMR and X-ray crystallography, to confirm the stereochemistry and structural integrity of the molecule. These findings are critical for ensuring the reproducibility and scalability of the synthesis process, which is essential for its industrial and pharmaceutical applications.

In the realm of medicinal chemistry, Borane,2-propen-1-ylbis[(1S,2R,3S,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-3-yl]- has shown promise as a key intermediate in the synthesis of bioactive molecules. A recent study in Bioorganic & Medicinal Chemistry Letters (2024) highlighted its utility in the construction of boron-containing compounds with potential anticancer activity. The researchers demonstrated that the borane moiety could enhance the binding affinity of these compounds to specific biological targets, thereby improving their therapeutic efficacy. This discovery opens new avenues for the development of boron-based drugs, which are increasingly recognized for their unique pharmacological properties.

Furthermore, the catalytic applications of Borane,2-propen-1-ylbis[(1S,2R,3S,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-3-yl]- have been explored in recent years. A study in ACS Catalysis (2023) reported its use as a chiral ligand in asymmetric hydrogenation reactions, which are pivotal in the production of enantiomerically pure pharmaceuticals. The compound's rigid bicyclic framework and borane functionality were found to significantly influence the stereoselectivity of the reactions, leading to higher yields of the desired enantiomers. These findings underscore the compound's potential in streamlining the synthesis of chiral drugs, which are often challenging to produce using conventional methods.

Despite these advancements, challenges remain in the widespread adoption of Borane,2-propen-1-ylbis[(1S,2R,3S,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-3-yl]-. Issues such as its stability under various reaction conditions and the cost of large-scale production need to be addressed. Ongoing research is focused on optimizing the compound's properties and developing more efficient synthetic protocols. Collaborative efforts between academia and industry are expected to drive further innovations in this area, paving the way for its broader application in chemical biology and drug discovery.

In conclusion, Borane,2-propen-1-ylbis[(1S,2R,3S,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-3-yl]- (CAS: 106356-53-0) represents a versatile and promising compound in the field of chemical biology and medicinal chemistry. Recent studies have elucidated its synthetic pathways, biological activities, and catalytic applications, highlighting its potential to contribute to the development of new therapeutic agents and synthetic methodologies. As research in this area continues to evolve, this compound is likely to play an increasingly important role in addressing some of the most pressing challenges in the pharmaceutical and chemical industries.

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