
CAS 16492-29-8
:6-Amino-2-chloro-4-pyrimidinecarboxylic acid
Description:
6-Amino-2-chloro-4-pyrimidinecarboxylic acid is a heterocyclic organic compound characterized by its pyrimidine ring structure, which includes an amino group and a chloro substituent. This compound features a carboxylic acid functional group, contributing to its acidic properties. The presence of the amino group enhances its potential for forming hydrogen bonds, making it a candidate for various biological activities. The chlorine atom introduces additional reactivity and can influence the compound's solubility and interaction with other molecules. Typically, compounds like this are of interest in medicinal chemistry and agricultural applications, often serving as intermediates in the synthesis of pharmaceuticals or agrochemicals. Its molecular structure allows for potential interactions with biological targets, which may lead to therapeutic effects. As with many pyrimidine derivatives, it may exhibit properties such as antimicrobial or antiviral activity, although specific biological activities would require empirical investigation. Safety and handling precautions should be observed due to the presence of chlorine and the potential for biological activity.
Formula:C5H4ClN3O2
InChI:InChI=1S/C5H4ClN3O2/c6-5-8-2(4(10)11)1-3(7)9-5/h1H,(H,10,11)(H2,7,8,9)
InChI key:InChIKey=UHGBKWYISOUYAE-UHFFFAOYSA-N
SMILES:C(O)(=O)C=1C=C(N)N=C(Cl)N1
Synonyms:- 4-Pyrimidinecarboxylic acid, 6-amino-2-chloro-
- 6-Amino-2-chloro-4-pyrimidinecarboxylic acid
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Found 2 products.
6-Amino-2-chloropyrimidine-4-carboxylic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C5H4ClN3O2Purity:Min. 95%Molecular weight:173.56 g/mol

