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CAS 925932-71-4

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C-(1,1-Dimethylethyl) N-(3-borylphenyl)-N-butylcarbamate

Description:
C-(1,1-Dimethylethyl) N-(3-borylphenyl)-N-butylcarbamate, with the CAS number 925932-71-4, is a chemical compound characterized by its unique structure that includes a carbamate functional group. This compound features a tert-butyl group (1,1-dimethylethyl) attached to the carbon atom of the carbamate, which contributes to its steric bulk and potentially influences its reactivity and solubility. The presence of a boryl group attached to a phenyl ring indicates that it may have applications in organoboron chemistry, possibly serving as a precursor for various synthetic pathways or as a reagent in cross-coupling reactions. The butyl group enhances its hydrophobic characteristics, which may affect its interaction with biological systems or its solubility in organic solvents. Overall, this compound's structure suggests potential utility in medicinal chemistry or materials science, particularly in the development of boron-containing compounds for various applications. Further studies would be necessary to fully elucidate its properties and potential uses.
Formula:C15H24BNO4
InChI:InChI=1S/C15H24BNO4/c1-5-6-10-17(14(18)21-15(2,3)4)13-9-7-8-12(11-13)16(19)20/h7-9,11,19-20H,5-6,10H2,1-4H3
InChI key:InChIKey=PWGLYYWIKQFCSS-UHFFFAOYSA-N
SMILES:N(C(OC(C)(C)C)=O)(CCCC)C1=CC(B(O)O)=CC=C1
Synonyms:
  • C-(1,1-Dimethylethyl) N-(3-borylphenyl)-N-butylcarbamate
  • Carbamic acid, N-(3-borylphenyl)-N-butyl-, C-(1,1-dimethylethyl) ester
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