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CAS 1310404-08-0

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1,1-Dimethylethyl N-[6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinyl]carbamate

Description:
1,1-Dimethylethyl N-[6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinyl]carbamate, identified by its CAS number 1310404-08-0, is a chemical compound characterized by its complex structure, which includes a carbamate functional group and a pyridine ring substituted with a boron-containing moiety. This compound is likely to exhibit properties typical of carbamates, such as potential biological activity, including herbicidal or pesticidal effects, due to its nitrogen-containing functional group. The presence of the dioxaborolane group suggests it may participate in boron chemistry, potentially influencing its reactivity and interactions in various chemical environments. Additionally, the dimethyl groups contribute to steric hindrance, which may affect its solubility and stability. Overall, this compound's unique structural features may render it useful in synthetic chemistry or agricultural applications, although specific reactivity and biological activity would require further investigation through empirical studies.
Formula:C16H25BN2O4
InChI:InChI=1S/C16H25BN2O4/c1-14(2,3)21-13(20)19-11-8-9-12(18-10-11)17-22-15(4,5)16(6,7)23-17/h8-10H,1-7H3,(H,19,20)
InChI key:InChIKey=FOJRYIYOPLHVMZ-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC=C(NC(OC(C)(C)C)=O)C=N2
Synonyms:
  • Carbamic acid, N-[6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinyl]-, 1,1-dimethylethyl ester
  • 1,1-Dimethylethyl N-[6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinyl]carbamate
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