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CAS 234108-73-7

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4-(Boc-amino)-2-chloropyridine

Description:
4-(Boc-amino)-2-chloropyridine is a chemical compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. The compound features a Boc (tert-butyloxycarbonyl) protecting group attached to an amino group, enhancing its stability and facilitating further chemical reactions. The presence of a chlorine atom at the 2-position of the pyridine ring introduces electrophilic characteristics, making it a useful intermediate in various synthetic pathways, particularly in medicinal chemistry and drug development. This compound is typically utilized in the synthesis of more complex molecules, including pharmaceuticals, due to its ability to undergo nucleophilic substitution reactions. Its solubility and reactivity can vary depending on the solvent and reaction conditions, and it is generally handled with standard laboratory safety precautions. As with many nitrogen-containing heterocycles, it may exhibit basic properties, allowing it to participate in acid-base reactions. Overall, 4-(Boc-amino)-2-chloropyridine serves as a versatile building block in organic synthesis.
Formula:C10H13ClN2O2
InChI:InChI=1/C10H13ClN2O2/c1-10(2,3)15-9(14)13-7-4-5-12-8(11)6-7/h4-6H,1-3H3,(H,12,13,14)
SMILES:CC(C)(C)OC(=Nc1ccnc(c1)Cl)O
Synonyms:
  • carbamic acid, N-(2-chloro-4-pyridinyl)-, 1,1-dimethylethyl ester
  • tert-Butyl (2-chloropyridin-4-yl)carbamate
  • tert-butyl N-(2-chloropyridin-4-yl)carbamate
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