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CAS 1310405-05-0

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

Description:
1,1-Dimethylethyl N-[2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinyl]carbamate, identified by its CAS number 1310405-05-0, is a chemical compound characterized by its complex structure, which includes a pyridine ring and a boron-containing moiety. This compound features a carbamate functional group, which is known for its applications in medicinal chemistry and as a building block in organic synthesis. The presence of the tetramethyl-1,3,2-dioxaborolane unit suggests potential reactivity and utility in various chemical transformations, particularly in the context of boron chemistry. The dimethyl group contributes to steric hindrance, which can influence the compound's reactivity and interaction with biological targets. Overall, this compound may exhibit interesting properties, making it a candidate for research in fields such as agrochemicals or pharmaceuticals, although specific biological activity and stability would require further investigation. Its unique structural features may also lend themselves to applications in materials science or catalysis.
Formula:C16H25BN2O4
InChI:InChI=1S/C16H25BN2O4/c1-14(2,3)21-13(20)19-11-9-8-10-18-12(11)17-22-15(4,5)16(6,7)23-17/h8-10H,1-7H3,(H,19,20)
InChI key:InChIKey=XCWXAPFZBSZJDT-UHFFFAOYSA-N
SMILES:N(C(OC(C)(C)C)=O)C1=C(B2OC(C)(C)C(C)(C)O2)N=CC=C1
Synonyms:
  • 1,1-Dimethylethyl N-[2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinyl]carbamate
  • Carbamic acid, N-[2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinyl]-, 1,1-dimethylethyl ester
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