CAS 1899-99-6
:2-chloro-4-methoxy-6-methyl-5-nitropyrimidine
Description:
2-Chloro-4-methoxy-6-methyl-5-nitropyrimidine is a heterocyclic organic compound characterized by its pyrimidine ring, which contains various substituents that influence its chemical properties and reactivity. The presence of a chlorine atom at the 2-position, a methoxy group at the 4-position, a methyl group at the 6-position, and a nitro group at the 5-position contributes to its unique chemical behavior. This compound is typically a yellow to orange solid and is soluble in organic solvents. Its nitro group can participate in electrophilic reactions, while the methoxy group can act as an electron-donating group, affecting the compound's reactivity. The chlorine atom introduces a halogen, which can enhance the compound's reactivity in nucleophilic substitution reactions. Due to these functional groups, 2-chloro-4-methoxy-6-methyl-5-nitropyrimidine may exhibit biological activity, making it of interest in pharmaceutical research. Safety data should be consulted, as compounds with nitro and chloro groups can pose health risks.
Formula:C6H6ClN3O3
InChI:InChI=1/C6H6ClN3O3/c1-3-4(10(11)12)5(13-2)9-6(7)8-3/h1-2H3
InChI key:PNVXPMQAFHWYMN-UHFFFAOYSA-N
SMILES:Cc1c(c(nc(Cl)n1)OC)N(=O)=O
Synonyms:- Pyrimidine, 2-Chloro-4-Methoxy-6-Methyl-5-Nitro-
- 2-Chloro-4-methoxy-6-methyl-5-nitropyrimidine
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