CAS 73-68-7

4-amino-2-methylpyrimidine-5-carbaldehyde

Description:

4-Amino-2-methylpyrimidine-5-carbaldehyde is an organic compound characterized by its pyrimidine ring structure, which includes an amino group and an aldehyde functional group. This compound features a methyl group at the second position of the pyrimidine ring, contributing to its unique reactivity and properties. The presence of the amino group makes it a potential candidate for various chemical reactions, including nucleophilic substitutions and coupling reactions, while the aldehyde group can participate in condensation reactions and serve as a precursor for further synthetic modifications. It is typically a solid at room temperature and may exhibit solubility in polar solvents due to the presence of the amino and aldehyde functionalities. This compound is of interest in medicinal chemistry and organic synthesis, as derivatives of pyrimidine are often found in pharmaceuticals and agrochemicals. Safety data should be consulted for handling, as with any chemical substance, to ensure proper precautions are taken.

Formula: C₆H₇N₃O

InChI: InChI=1/C6H7N3O/c1-4-8-2-5(3-10)6(7)9-4/h2-3H,1H3,(H2,7,8,9)

SMILES: Cc1ncc(C=O)c(=N)[nH]1

Synonyms:

• 5-Pyrimidinecarboxaldehyde, 4-Amino-2-Methyl-
• 4-Amino-2-methylpyrimidine-5-carbaldehyde

4-Amino-2-methylpyrimidine-5-carbaldehyde

CAS: 73-68-7

Formula: C₆H₇N₃O

Purity: 98%

Color and Shape: Solid

Molecular weight: 137.1393

Ref: IN-DA005LTB

4-Amino-2-methyl-5-pyrimidinecarboxaldehyde

CAS: 73-68-7

4-Amino-2-methyl-5-pyrimidinecarboxaldehyde

Purity: 98%

Ref: 54-OR1039923

4-AMINO-2-METHYLPYRIMIDINE-5-CARBALDEHYDE

CAS: 73-68-7

Formula: C₆H₇N₃O

Purity: 98%

Molecular weight: 137.142

Ref: 10-F303805

4-Amino-5-formyl-2-methylpyrimidine

CAS: 73-68-7

4-Amino-5-formyl-2-methylpyrimidine is an intermediate in the metabolism of pargyline and is able to inhibit oxidative enzymes. It has also been shown to be a potent inhibitor of the oxidation of aldehydes, ketones, and alcohols to their corresponding carboxylic acids. 4-Amino-5-formyl-2-methylpyrimidine is capable of inhibiting the oxidation of acetonitrile to nitrile with an IC50 value of 3.6 mM. This compound has not been shown to be an inhibitor of cytochrome P450 or monoamine oxidase, but it inhibits pyridoxal phosphate (a cofactor for tyrosine hydroxylase) and can therefore inhibit dopamine synthesis. The postulated mechanism is that 4-amino-5 formyl 2MMP binds to the active site on pyridoxal phosphate, thereby preventing its conversion into

Formula: C₆H₇N₃O

Purity: Min. 95%

Molecular weight: 137.14 g/mol

Ref: 3D-AAA07368