Your Location:Home >Products >Intermediates >215527-70-1

Phenyl-d5-boronic acid

  • CAS:215527-70-1
  • MF:C6H2BD5O2
  • Purity:99%
  • Molecular Weight:126.892
Get the best price

Product Details

  • CAS: 215527-70-1
  • MF: C6H2BD5O2
  • High Quality Chinese Factory supply 215527-70-1 Phenyl-d5-boronic acid

    • Molecular Formula:C6H2BD5O2
    • Molecular Weight:126.892
    • Vapor Pressure:0.00446mmHg at 25°C 
    • Melting Point:217-220 °C(lit.)  
    • Boiling Point:265.9°C at 760 mmHg 
    • Flash Point:114.6°C 
    • PSA:40.46000 
    • Density:1.18g/cm3 
    • LogP:-0.63360 

    PHENYL-D5-BORONIC ACID(Cas 215527-70-1) Usage

    InChI:InChI=1/C6H7BO2/c8-7(9)6-4-2-1-3-5-6/h1-5,8-9H/i1D,2D,3D,4D,5D

    215527-70-1 Relevant articles

    Domino Carbopalladation/C-H Activation as a Quick Access to Polycyclic Frameworks

    Saha, Nemai,Wang, Haiwen,Zhang, Shengyi,Du, Yongliang,Zhu, Daqian,Hu, Yumin,Huang, Peng,Wen, Shijun

    , p. 712 - 715 (2018)

    A new type of domino reaction for synthe...

    FORMATION OF BOTH METHYLENEDIOXY GROUPS IN THE ALKALOID (S)-STYLOPINE ISCATALYZED BY CYTOCHROME P-450 ENZYMES

    Bauer, W.,Zenk, M.H.

    , p. 5257 - 5260 (1989)

    Two higly stereospecific microsomal cyto...

    Electrochemically enabled rhodium-catalyzed [4 + 2] annulations of arenes with alkynes

    Chen, Jia-Yi,Li, Ming,Li, Rui-Tao,Ma, Qiang,Ni, Shao-Fei,Wang, Zi-Chen,Wen, Li-Rong,Zhang, Lin-Bao

    supporting information, p. 9515 - 9522 (2021/12/09)

    Herein, electrochemically driven, Rh(iii...

    Pd(II)-Catalyzed Synthesis of Alkylidene Phthalides via a Decarbonylative Annulation Reaction

    Borthakur, Somadrita,Baruah, Swagata,Sarma, Bipul,Gogoi, Sanjib

    supporting information, p. 2768 - 2771 (2019/04/16)

    An unprecedented Pd(II)-catalyzed decarb...

    Deuterated phenyl containing triazine compound and applications thereof, and organic electroluminescent device

    -

    Paragraph 0120; 0121; 0126; 0127, (2019/04/10)

    The invention relates to the field of or...

    Arylation/Intramolecular Conjugate Addition of 1,6-Enynes Enabled by Manganese(I)-Catalyzed C-H Bond Activation

    Tan, Yun-Xuan,Liu, Xing-Yu,Zhao, Yi-Shuang,Tian, Ping,Lin, Guo-Qiang

    supporting information, p. 5 - 9 (2018/11/23)

    An arylation/intramolecular conjugate ad...

    215527-70-1 Process route

    Triisopropyl borate
    5419-55-6

    Triisopropyl borate

    bromobenzene-d5
    4165-57-5

    bromobenzene-d5

    2,3,4,5,6-pentadeuteriumbenzeneboronic acid
    215527-70-1

    2,3,4,5,6-pentadeuteriumbenzeneboronic acid

    Conditions
    Conditions Yield
    bromobenzene-d5; With n-butyllithium; In tetrahydrofuran; hexane; at -78 ℃; for 2h; Inert atmosphere;
    Triisopropyl borate; In tetrahydrofuran; hexane; at -78 - 20 ℃;
    84%
    bromobenzene-d5; With n-butyllithium; In tetrahydrofuran; hexane; at -78 ℃; for 2h; Inert atmosphere;
    Triisopropyl borate; In tetrahydrofuran; hexane; at 20 ℃; for 3h;
    64%
    bromobenzene-d5; With n-butyllithium; In tetrahydrofuran; at -78 ℃; for 2.5h; Inert atmosphere;
    Triisopropyl borate; In tetrahydrofuran; at -78 - 20 ℃; Inert atmosphere;
    With hydrogenchloride; water; In tetrahydrofuran; at 20 ℃; for 3h;
    bromobenzene-d5; With n-butyllithium; In tetrahydrofuran; at -78 ℃; for 2.5h; Inert atmosphere; Schlenk technique;
    Triisopropyl borate; In tetrahydrofuran; at -78 - 20 ℃; Inert atmosphere; Schlenk technique;
    With hydrogenchloride; In tetrahydrofuran; water; at 20 ℃; for 3h; Inert atmosphere; Schlenk technique;
    bromobenzene-d5; With n-butyllithium; In tetrahydrofuran; hexane; at -78 ℃; for 0.25h; Inert atmosphere;
    Triisopropyl borate; In tetrahydrofuran; hexane; at 25 ℃; for 0.333333h; Inert atmosphere;
    bromobenzene-d5; With n-butyllithium; In tetrahydrofuran; at -78 ℃; for 1.25h; Inert atmosphere;
    Triisopropyl borate; In tetrahydrofuran; at 20 ℃; for 12h; Inert atmosphere;
    bromobenzene-d5; With n-butyllithium; In tetrahydrofuran; at -78 ℃; for 0.5h; Inert atmosphere;
    Triisopropyl borate; In tetrahydrofuran; at -78 ℃; for 2h; Inert atmosphere;
    bromobenzene-d5; With n-butyllithium; In tetrahydrofuran; at -78 ℃; for 2.5h; Inert atmosphere;
    Triisopropyl borate; In tetrahydrofuran; at -78 - 20 ℃; Inert atmosphere;
    bromobenzene-d5; With n-butyllithium; In tetrahydrofuran; at -78 ℃; for 2h; Inert atmosphere;
    Triisopropyl borate; In tetrahydrofuran; at -78 - 20 ℃; Inert atmosphere;
    triethyl borate
    150-46-9

    triethyl borate

    bromobenzene-d5
    4165-57-5

    bromobenzene-d5

    2,3,4,5,6-pentadeuteriumbenzeneboronic acid
    215527-70-1

    2,3,4,5,6-pentadeuteriumbenzeneboronic acid

    Conditions
    Conditions Yield
    bromobenzene-d5; With tert.-butyl lithium; In tetrahydrofuran; at -78 ℃; for 0.5h;
    triethyl borate; In tetrahydrofuran; at -78 - 20 ℃; for 12h;
    With hydrogenchloride; In tetrahydrofuran; water; for 1h;
    69%

    215527-70-1 Upstream products

    • 41646-18-8
      41646-18-8

      (6aS)-6,11,12,14-tetrahydro-9-methoxy-6aH-[1,3]dioxolo[4,5-h]isoquinolino[2,1-b]isoquinolin-8-ol

    • 4165-57-5
      4165-57-5

      bromobenzene-d5

    • 150-46-9
      150-46-9

      triethyl borate

    • 525598-50-9
      525598-50-9

      C8H6(2)H5BO2

    215527-70-1 Downstream products

    • 178110-60-6
      178110-60-6

      4-tert-butyl-2,6-di(phenyl-d5)aniline

    • 178110-59-3
      178110-59-3

      (2,4-Diphenyl-d5)-6-tert-butylaniline

    • 501422-70-4
      501422-70-4

      4-acetyl-2,6-di(phenyl-d5)aniline

    • 215527-72-3
      215527-72-3

      4-(phenyl-d5)aniline

    Antioxidant BHT 264

    CAS:128-37-0

    Purity:99%

    Contact Now

    We will contact you as soon as possible


    提交