1195-07-9

Usage

Uses

Used in Pharmaceutical Research and Development:
5-(Aminomethyl)-2-Methylpyrimidin-4-amine hydrochloride is used as an intermediate in the synthesis of antiviral and anticancer drugs for its potential therapeutic properties.
Used in Biochemical Research:
In the field of biochemistry, 5-(Aminomethyl)-2-Methylpyrimidin-4-amine hydrochloride is used as a research tool to study the interactions of pyrimidine-based compounds with biological systems.
Used in Molecular Biology:
5-(Aminomethyl)-2-Methylpyrimidin-4-amine hydrochloride is employed as a component in molecular biology experiments, potentially aiding in the understanding of nucleic acid structures and functions.
Used in Medicinal Chemistry:
5-(Aminomethyl)-2-Methylpyrimidin-4-amine hydrochloride is utilized as a building block in the design and synthesis of novel pharmaceutical compounds targeting various diseases.

Upstream product

• 7647-01-0 hydrogenchloride 
• 7732-18-5 water 
• 2421-50-3 N-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-N-(4-hydroxy-1-methyl-2-thiocyanato-but-1-en-t-yl)-formamide 
• 32795-64-5 5-(2-hydroxy-ethyl)-4-methyl-3H-thiazol-2-one 

Downstream Products

• 7403-34-1 7-methyl-3,4-dihydro-1H-pyrimido[4,5-d]pyrimidine-2-thione 
• 109039-39-6 3-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-5-(2-hydroxy-ethyl)-4-phenyl-3H-thiazole-2-thione 
• 1344707-26-1 (R/S)-N-((4-amino-2-methylpyrimidin-5-yl)methyl)-2-hydroxy-2-(4-(5-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-1,2,4-oxadiazol-3-yl)phenyl)acetamide 
• 1246636-78-1 methyl 2-(4-(6-((4-amino-2-methylpyrimidin-5-yl)methylamino)pyrimidin-4-yloxy)phenyl)acetate 
• 109653-94-3 3-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-5-(2-hydroxy-ethyl)-4-phenyl-thiazolium; chloride-hydrochloride 
• 92-35-3 thiochrome 
• 66840-33-3 7-methyl-3,4-dihydro-1H-pyrimido[4,5-d]pyrimidin-2-one 
• 25526-81-2 5-bromomethyl-2-methyl-pyrimidin-4-ylamine 
• 490-82-4 thiamine thiazolone 
• 73-66-5 5-ethoxymethyl-2-methyl-pyrimidin-4-ylamine 

Relevant academic research and scientific papers

2-Alkyl-4-amino-5-aminomethylpyrimidines

A novel 2-lower alkyl-4-amino-5-substituted iminopyrimidine compound represented by the formula: STR1 wherein R is a lower alkyl, and Y is hydroxyl or amino which may be protected or a salt thereof is obtainable by allowing a formylpyrimidine compound represented by the formula: STR2 wherein R is a lower alkyl to react with a compound represented by the formula H2 N--Y, wherein Y is hydroxyl or amino which may be protected, or a salts thereof. The iminopyrimidine compound gives the known pyrimidine compound represented by the formula: STR3 wherein R is as defined above in high yield. Therefor, the process is very useful as an industrial production method.