TIMTEC-BB SBB004134;2-amino-4-chloro-6-methyl-pyrimidin;2-Pyrimidinamine, 4-chloro-6-methyl-;2-AMINO-4-CHLORO-6-METHYLPYRIMIDINE (ACLP);2-Amino-4-chloro-6-methylpyrimidine ,97%;4-Chloro-6-methyl-pyrimidine-2-amine;2-Amino-4-chloro-6-methylpyrimidine,98%;AMR human cell line
2-Amino-4-chloro-6-methylpyrimidine Usage And Synthesis
Chemical Properties
WHITE TO LIGHT YELLOW NEEDLE-LIKE CRYST. POWDER
Uses
2-Amino-4-chloro-6-methylpyrimidine was used to study the influence of chlorine substitution in pyrimidine ring on proton donor ability of amino group in 2-aminopyrimidine.
Definition
ChEBI: An aminopyrimidine compound having its amino group at position 2 and chloro and methyl substituents at positions 4 and 6 respectively.
General Description
2-Amino-4-chloro-6-methylpyrimidine is a nitification inhibitor.
Purification Methods
Recrystallise it from EtOH. [Beilstein 24 H 84.]
2-Amino-4-chloro-6-methylpyrimidine Preparation Products And Raw materials