CAS 34844-88-7
:N-Cyclopentyl-4-pyridinamine
Description:
N-Cyclopentyl-4-pyridinamine, identified by its CAS number 34844-88-7, is an organic compound characterized by its pyridine and cyclopentyl functional groups. It features a pyridine ring substituted with an amino group at the 4-position and a cyclopentyl group at the nitrogen atom. This compound is typically a solid at room temperature and exhibits moderate solubility in polar solvents due to the presence of the amino group, which can engage in hydrogen bonding. Its structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as pyridine derivatives are often associated with biological activity. The cyclopentyl group may influence the compound's lipophilicity and receptor binding properties. Additionally, N-Cyclopentyl-4-pyridinamine may undergo typical organic reactions such as alkylation, acylation, or coupling reactions, making it a versatile intermediate in synthetic organic chemistry. Safety data should be consulted for handling and storage, as with all chemical substances, to ensure proper laboratory practices.
Formula:C10H14N2
InChI:InChI=1S/C10H14N2/c1-2-4-9(3-1)12-10-5-7-11-8-6-10/h5-9H,1-4H2,(H,11,12)
InChI key:InChIKey=ZYPKTMZFRMKZMM-UHFFFAOYSA-N
SMILES:N(C=1C=CN=CC1)C2CCCC2
Synonyms:- 4-Pyridinamine, N-cyclopentyl-
- Pyridine, 4-(cyclopentylamino)-
- N-Cyclopentyl-4-pyridinamine
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Found 1 products.
N-Cyclopentylpyridin-4-amine
CAS:<p>N-Cyclopentylpyridin-4-amine is a chemical compound with the formula CH(NH)CHCClN. It is an alkylation agent that consists of a cyclopentanol group and a pyridine ring. The cyclopentanol group reacts with electrophiles such as 2-propanol and 4-aminopyridine to form a cyclohexanol derivative. This reaction is catalyzed by sulfuric acid. N-Cyclopentylpyridin-4-amine has been used for the preparation of cyclopentanols, which are valuable intermediates in organic synthesis.</p>Formula:C10H14N2Purity:Min. 95%Molecular weight:162.23 g/mol
