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CAS 1310405-34-5

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1,1-Dimethylethyl 4-[2-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]ethyl]-1-piperidinecarboxylate

Description:
1,1-Dimethylethyl 4-[2-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]ethyl]-1-piperidinecarboxylate, identified by its CAS number 1310405-34-5, is a chemical compound characterized by its complex structure that includes a piperidine ring, a phenoxy group, and a boron-containing moiety. This compound features a tert-butyl group, which contributes to its steric bulk and may influence its reactivity and solubility. The presence of the dioxaborolane unit suggests potential applications in organic synthesis, particularly in cross-coupling reactions or as a reagent in various chemical transformations. The compound's functional groups indicate it may exhibit specific interactions with biological targets, making it of interest in medicinal chemistry. Its solubility, stability, and reactivity would depend on the solvent and conditions used, and it may require careful handling due to the presence of boron, which can be sensitive to moisture and air. Overall, this compound represents a versatile structure with potential applications in both synthetic and pharmaceutical chemistry.
Formula:C24H38BNO5
InChI:InChI=1S/C24H38BNO5/c1-22(2,3)29-21(27)26-14-11-18(12-15-26)13-16-28-20-10-8-9-19(17-20)25-30-23(4,5)24(6,7)31-25/h8-10,17-18H,11-16H2,1-7H3
InChI key:InChIKey=FFHPDWSFIHNDEZ-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC(OCCC3CCN(C(OC(C)(C)C)=O)CC3)=CC=C2
Synonyms:
  • 1,1-Dimethylethyl 4-[2-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]ethyl]-1-piperidinecarboxylate
  • 1-Piperidinecarboxylic acid, 4-[2-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]ethyl]-, 1,1-dimethylethyl ester
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