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CAS 1310404-53-5

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

Description:
1,1-Dimethylethyl N-[6-chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinyl]carbamate, identified by its CAS number 1310404-53-5, is a chemical compound characterized by its complex structure, which includes a pyridine ring, a carbamate functional group, and a boron-containing moiety. The presence of the chloro substituent and the bulky dimethyl groups contributes to its unique reactivity and steric properties. This compound is likely to exhibit specific biological activities, making it of interest in pharmaceutical research, particularly in the development of agrochemicals or medicinal agents. Its boron-containing structure may also suggest potential applications in materials science or catalysis. The stability and solubility of this compound can be influenced by its functional groups, and it may undergo various chemical reactions typical of carbamates, such as hydrolysis or nucleophilic substitution. Overall, the characteristics of this compound make it a subject of interest for further investigation in both synthetic and applied chemistry contexts.
Formula:C16H24BClN2O4
InChI:InChI=1S/C16H24BClN2O4/c1-14(2,3)22-13(21)20-10-8-11(12(18)19-9-10)17-23-15(4,5)16(6,7)24-17/h8-9H,1-7H3,(H,20,21)
InChI key:InChIKey=DCHNZMSXFZTTID-UHFFFAOYSA-N
SMILES:ClC1=C(B2OC(C)(C)C(C)(C)O2)C=C(NC(OC(C)(C)C)=O)C=N1
Synonyms:
  • 1,1-Dimethylethyl N-[6-chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinyl]carbamate
  • Carbamic acid, N-[6-chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinyl]-, 1,1-dimethylethyl ester
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