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CAS 1346809-09-3

:

1,1-Dimethylethyl N-[(5-bromo-3-pyridinyl)methyl]-N-(2-methoxyethyl)carbamate

Description:
1,1-Dimethylethyl N-[(5-bromo-3-pyridinyl)methyl]-N-(2-methoxyethyl)carbamate, with the CAS number 1346809-09-3, is a chemical compound characterized by its complex structure, which includes a carbamate functional group. This compound features a branched alkyl group (1,1-dimethylethyl) that contributes to its steric hindrance, potentially influencing its reactivity and solubility. The presence of a pyridine ring, specifically substituted with a bromine atom, suggests potential biological activity, as pyridine derivatives are often found in pharmaceuticals. The methoxyethyl substituent enhances its solubility in organic solvents and may affect its interaction with biological targets. The compound's molecular structure indicates it may exhibit specific properties such as moderate to high lipophilicity, which can influence its absorption and distribution in biological systems. Overall, this compound's unique combination of functional groups and substituents suggests potential applications in medicinal chemistry or agrochemicals, although specific biological activity would require further investigation through experimental studies.
Formula:C14H21BrN2O3
InChI:InChI=1S/C14H21BrN2O3/c1-14(2,3)20-13(18)17(5-6-19-4)10-11-7-12(15)9-16-8-11/h7-9H,5-6,10H2,1-4H3
InChI key:InChIKey=WZPASIJVXCRJEJ-UHFFFAOYSA-N
SMILES:C(N(C(OC(C)(C)C)=O)CCOC)C=1C=C(Br)C=NC1
Synonyms:
  • 1,1-Dimethylethyl N-[(5-bromo-3-pyridinyl)methyl]-N-(2-methoxyethyl)carbamate
  • Carbamic acid, N-[(5-bromo-3-pyridinyl)methyl]-N-(2-methoxyethyl)-, 1,1-dimethylethyl ester
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