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Chemical Structure| 1186638-14-1 Chemical Structure| 1186638-14-1

Structure of 1186638-14-1

Chemical Structure| 1186638-14-1

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Product Details of [ 1186638-14-1 ]

CAS No. :1186638-14-1
Formula : C13H18BNO6
M.W : 295.10
SMILES Code : OB(C1=CC=C(C(OC)=O)C=C1NC(OC(C)(C)C)=O)O
MDL No. :MFCD18384189

Safety of [ 1186638-14-1 ]

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 [ 1186638-14-1 ]

* 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 [ 1186638-14-1 ]

[ 1186638-14-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 380430-55-7 ]
  • [ 24424-99-5 ]
  • [ 1186638-14-1 ]
YieldReaction ConditionsOperation in experiment
With triethylamine;dmap; In acetonitrile; at 40℃; A solution of <strong>[380430-55-7]2-amino-4-(methoxycarbonyl)phenylboronic acid hydrochloride</strong> (commercially available) (1.0 eq.), triethylamine (3.0 eq ), di-foert-butyl dicarbonate (1.1 eq ), and DMAP (0.1 eq.) in CH3CN (0.3 M) was stirred at 400C overnight. After cooling to ambient temperature, the reaction mixture was concentrated en vaccuo to obtain a crude residue. The crude material was purified by flash chromatography on a COMBIFLASH.(R). system (ISCO) using 0-30percent MeOH/DCM to give 2-(tert-butoxycarbonylamino)-4-(methoxycarbonyl)phenylboronic acid as a brown solid.
 

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