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CAS 175277-10-8

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1-(tert-butyl)-3-methyl-1H-pyrazole-5-carbonyl chloride

Description:
1-(tert-butyl)-3-methyl-1H-pyrazole-5-carbonyl chloride is a chemical compound characterized by its unique pyrazole structure, which features a tert-butyl group and a methyl group attached to the pyrazole ring. This compound is typically a colorless to pale yellow liquid or solid, depending on its state at room temperature. It is known for its reactivity due to the presence of the carbonyl chloride functional group, which can participate in various nucleophilic substitution reactions. The tert-butyl group contributes to its steric bulk, influencing its chemical reactivity and solubility properties. This compound is often utilized in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to its ability to serve as an intermediate in the formation of more complex molecules. Additionally, it may exhibit specific biological activities, making it of interest in medicinal chemistry. Proper handling and storage are essential, as carbonyl chlorides can be hazardous, requiring precautions to avoid exposure to moisture and reactive substances.
Formula:C9H13ClN2O
InChI:InChI=1/C9H13ClN2O/c1-6-5-7(8(10)13)12(11-6)9(2,3)4/h5H,1-4H3
SMILES:Cc1cc(C(=O)Cl)n(C(C)(C)C)n1
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