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CAS 116026-95-0

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1,1-Dimethylethyl N-(4-formyl-3-pyridinyl)carbamate

Description:
1,1-Dimethylethyl N-(4-formyl-3-pyridinyl)carbamate, identified by its CAS number 116026-95-0, is a chemical compound that features a carbamate functional group linked to a pyridine derivative. This compound typically exhibits characteristics associated with both carbamates and pyridine derivatives, including potential biological activity and solubility in organic solvents. The presence of the dimethyl group suggests steric hindrance, which may influence its reactivity and interaction with biological targets. The formyl group on the pyridine ring can participate in various chemical reactions, such as nucleophilic attacks or condensation reactions, making it a versatile intermediate in organic synthesis. Additionally, the compound may exhibit specific pharmacological properties, depending on its structure and substituents, which could be of interest in medicinal chemistry. Overall, this compound's unique structural features contribute to its potential applications in various fields, including pharmaceuticals and agrochemicals.
Formula:C11H14N2O3
InChI:InChI=1S/C11H14N2O3/c1-11(2,3)16-10(15)13-9-6-12-5-4-8(9)7-14/h4-7H,1-3H3,(H,13,15)
InChI key:InChIKey=YLKONQAWPOHLPX-UHFFFAOYSA-N
SMILES:N(C(OC(C)(C)C)=O)C=1C(C=O)=CC=NC1
Synonyms:
  • (4-Formyl-Pyridin-3-Yl)-Carbamic Acid Tert-Butyl Ester
  • 1,1-Dimethylethyl N-(4-formyl-3-pyridinyl)carbamate
  • 3-Aminopyridine-4-Carboxaldehyde, 3-Boc Protected
  • 3-Aminopyridine-4-carboxaldehyde, 3-BOC protected 95%
  • Carbamic acid, (4-formyl-3-pyridinyl)-, 1,1-dimethylethyl ester
  • Carbamic acid, N-(4-formyl-3-pyridinyl)-, 1,1-dimethylethyl ester
  • N-(4-formyl-3-pyridinyl)-Carbamic acid,1,1-dimethylethyl ester
  • N-Boc-3-Amino-4-Pyridine Carboxyaldehyde
  • N-Boc-3-amino-4-pyridine carboxzyaldehyde
  • tert-Butyl (4-formylpyridin-3-yl)carbamate
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