CAS 1142192-48-0

1,1-Dimethylethyl N-[(6-bromo-2-chloro-3-pyridinyl)methyl]carbamate

Description:

1,1-Dimethylethyl N-[(6-bromo-2-chloro-3-pyridinyl)methyl]carbamate, identified by its CAS number 1142192-48-0, is a chemical compound characterized by its unique structure that includes a carbamate functional group and a pyridine ring substituted with bromine and chlorine. This compound typically exhibits properties associated with both the carbamate and pyridine moieties, such as potential biological activity and solubility in organic solvents. The presence of halogen substituents (bromine and chlorine) on the pyridine ring may influence its reactivity and interaction with biological targets, making it of interest in medicinal chemistry and agrochemical applications. Additionally, the tert-butyl group (1,1-dimethylethyl) contributes to the compound's steric bulk, which can affect its pharmacokinetics and binding affinity. Overall, this compound's characteristics suggest it may have applications in various fields, including pharmaceuticals and crop protection, although specific biological activities and safety profiles would require further investigation.

Formula: C₁₁H₁₄BrClN₂O₂

InChI: InChI=1S/C11H14BrClN2O2/c1-11(2,3)17-10(16)14-6-7-4-5-8(12)15-9(7)13/h4-5H,6H2,1-3H3,(H,14,16)

InChI key: InChIKey=ZPJUAFUDQXGVRA-UHFFFAOYSA-N

SMILES: C(NC(OC(C)(C)C)=O)C1=C(Cl)N=C(Br)C=C1

Synonyms:

• 1,1-Dimethylethyl N-[(6-bromo-2-chloro-3-pyridinyl)methyl]carbamate
• Carbamic acid, N-[(6-bromo-2-chloro-3-pyridinyl)methyl]-, 1,1-dimethylethyl ester
• tert-Butyl (6-bromo-2-chloropyridin-3-yl)methylcarbamate
• tert-butyl N-[(6-bromo-2-chloropyridin-3-yl)methyl]carbamate