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Chemical Structure| 15961-35-0 Chemical Structure| 15961-35-0

Structure of 15961-35-0

Chemical Structure| 15961-35-0

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Product Details of [ 15961-35-0 ]

CAS No. :15961-35-0
Formula : C12H17BO2
M.W : 204.07
SMILES Code : CC1CC(C)(C)OB(C2=CC=CC=C2)O1
MDL No. :MFCD08436975

Safety of [ 15961-35-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 15961-35-0 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 15961-35-0 ]

[ 15961-35-0 ] Synthesis Path-Downstream   1~6

  • 1
  • [ 230299-21-5 ]
  • [ 1538-62-1 ]
  • [ 15961-35-0 ]
YieldReaction ConditionsOperation in experiment
83% With bis-triphenylphosphine-palladium(II) chloride; In 1,2-dimethoxyethane; at 60℃; for 12h; General procedure: A solution of triarylantimony diacetate (1: 0.5mmol), tetra(alkoxo)diboron (11: 1.5mmol), and dichlorobis(triphenylphosphine)palladium (II) (0.005mmol) in DME (5mL) was stirred at 60 °C for 12h under air atmosphere. After dilution with CH2Cl2 (30mL) and water (20mL), the reaction mixture was separated and the aqueous layer was extracted with CH2Cl2 (30mL×2). The combined organic layer was washed with brine, dried over anhydrous MgSO4 and concentrated under reduced pressure. The residue was purified by column chromatograph on silica gel to give arylboronates (12, 14?23). The products were confirmed by comparison of NMR data and MS spectra with that in the literature.
  • 2
  • [ 230299-21-5 ]
  • [ 14190-17-1 ]
  • [ 15961-35-0 ]
  • 5
  • [ 230299-21-5 ]
  • [ 455-32-3 ]
  • [ 15961-35-0 ]
  • 6
  • [ 230299-21-5 ]
  • C42H71FNiP2 [ No CAS ]
  • [ 15961-35-0 ]
 

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