223259-63-0

  • Product Name:1,1'-SPIROBIINDANE-7,7'-DIOL
  • Molecular Formula:C17H16 O2
  • Purity:99%
  • Molecular Weight:252.313
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Product Details

  • CasNo: 223259-63-0
  • Molecular Formula: C17H16 O2
  • Buy Reliable Quality High Purity 223259-63-0 with Best Price, Factory sells Top 223259-63-0 In Stock

    • Molecular Formula:C17H16O2
    • Molecular Weight:252.313
    • Melting Point:155-156℃ 
    • Boiling Point:433.0±45.0 °C(Predicted) 
    • PKA:9.70±0.20(Predicted) 
    • Flash Point:208.9oC 
    • PSA:40.46000 
    • Density:1.34±0.1 g/cm3(Predicted) 
    • LogP:3.27630 

    1,1'-SPIROBIINDANE-7,7'-DIOL (Cas 223259-63-0) Usage

    General Description

    1,1'-SPIROBIINDANE-7,7'-DIOL, also known as 3,3'-spirobi[1,2-dihydroindene]-4,4'-diol, is a chemical compound with the molecular formula C17H16O2 and a molecular weight of 252.31 grams per mole. It is a spiro compound, which means it contains two indene rings that are fused together with hydroxyl (OH) groups at positions 7 and 7' on the indene rings. It is a diol, meaning it has two hydroxyl groups (-OH) in its structure.

    Uses

    1,1'-SPIROBIINDANE-7,7'-DIOL may have various applications in chemical and pharmaceutical research, and its specific structure and functional groups can make it a valuable building block for the synthesis of more complex organic molecules.

    223259-63-0 Relevant articles

    A ligand synthesis of butadiene adhesive

    -

    , (2019/06/05)

    The invention relates to a synthesis met...

    Chiral oligomers of spiro-salencobalt(III)X for catalytic asymmetric cycloaddition of epoxides with CO2

    Zhu, Zhouhe,Zhang, Yuqian,Wang, Kai,Fu, Xiying,Chen, Fengjuan,Jing, Huanwang

    , p. 50 - 53 (2016/05/10)

    Several new chiral oligomers of spiro-sa...

    Chiral ligand 1,1'-spirobiindane-7,7'-diol synthesis method

    -

    Paragraph 0025, (2017/02/28)

    The present invention discloses a chiral...

    Phosphoric Acid-Catalyzed Asymmetric Synthesis of SPINOL Derivatives

    Li, Shaoyu,Zhang, Ji-Wei,Li, Xian-Lin,Cheng, Dao-Juan,Tan, Bin

    supporting information, p. 16561 - 16566 (2016/12/27)

    Axially chiral 1,1′-spirobiindane-7,7′-d...

    223259-63-0 Process route

    7,7'-dimethoxy-1,1'-spirobiindane
    223137-81-3,636601-25-7

    7,7'-dimethoxy-1,1'-spirobiindane

    (R)-2,2',3,3'-tetrahydro-1,1'-spirobi[indene]-7,7'-diol
    223137-87-9,223259-62-9,223259-63-0

    (R)-2,2',3,3'-tetrahydro-1,1'-spirobi[indene]-7,7'-diol

    Conditions
    Conditions Yield
    With boron tribromide; In dichloromethane; at -78 - 20 ℃;
    85%
    With boron tribromide; In dichloromethane; at -78 - 20 ℃;
     
    With tetrabutylammomium bromide; hydrogen bromide; at 105 ℃;
    57 g
    (S)-4,4'-dibromo-2,2',3,3'-tetrahydro-1,1'-spirobi[indene]-7,7'-diol
    636601-27-9,681481-91-4,681481-94-7

    (S)-4,4'-dibromo-2,2',3,3'-tetrahydro-1,1'-spirobi[indene]-7,7'-diol

    2,2′,3,3′-tetrahydro-1,1′-spirobi[indene]-7,7′-diol
    223137-87-9,223259-62-9,223259-63-0

    2,2′,3,3′-tetrahydro-1,1′-spirobi[indene]-7,7′-diol

    Conditions
    Conditions Yield
    With 5%-palladium/activated carbon; hydrogen; triethylamine; In tetrahydrofuran; water; at 20 ℃; for 12h;
    98%

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