CAS 1886-34-6

N-[(4-amino-2-methylpyrimidin-5-yl)methyl]formamide

Description:

N-[(4-amino-2-methylpyrimidin-5-yl)methyl]formamide, with the CAS number 1886-34-6, is an organic compound characterized by its pyrimidine ring structure, which includes an amino group and a methyl group at specific positions. This compound features a formamide functional group, indicating the presence of a carbonyl group (C=O) directly attached to a nitrogen atom (N). The molecular structure suggests it may exhibit polar characteristics due to the presence of both the formamide and amino groups, which can engage in hydrogen bonding. This property may influence its solubility in polar solvents, such as water. Additionally, the compound may have biological significance, potentially serving as an intermediate in the synthesis of pharmaceuticals or agrochemicals. Its reactivity can be attributed to the functional groups present, allowing for various chemical transformations. Overall, N-[(4-amino-2-methylpyrimidin-5-yl)methyl]formamide is a compound of interest in both synthetic chemistry and medicinal applications.

Formula: C₇H₁₀N₄O

InChI: InChI=1/C7H10N4O/c1-5-10-3-6(2-9-4-12)7(8)11-5/h3-4H,2H2,1H3,(H,9,12)(H2,8,10,11)

InChI key: InChIKey=PVWNFAGYFUUDRC-UHFFFAOYSA-N

SMILES: C(NC=O)C=1C(N)=NC(C)=NC1

Synonyms:

• 2-Methyl-4-amino-5-(formylaminomethyl)pyrimidine
• 4-AMino-5-(forMaMidoMethyl)-2-MethylpyriMidine
• 4-Amino-5-((formylamino)methyl)-2-methylpyrimidine
• N-[(4-Amino-2-methyl-5-pyrimidinyl)methyl]formamide
• S-((4-Amino-2-methylpyrimidin-5-yl)methyl) formamide
• formamide, N-[(4-amino-2-methyl-5-pyrimidinyl)methyl]-
• N-[(4-Amino-2-methylpyrimidin-5-yl)methyl]formamide
• synthesis-003
• synthesis-1-003
• Thiamine Impurity 7
• Cocarboxylase Tetrahydrate Impurity 2

4-Amino-5-(formamidomethyl)-2-methylpyrimidine

CAS: 1886-34-6

Formula: C₇H₁₀N₄O

Purity: 95%

Color and Shape: Solid

Molecular weight: 166.1805

Ref: IN-DA00ADW0

4-Amino-5-(formamidomethyl)-2-methylpyrimidine

CAS: 1886-34-6

4-Amino-5-(formamidomethyl)-2-methylpyrimidine

Purity: 95%

Ref: 54-OR1038572

Thiamine Impurity 20

CAS: 1886-34-6

Formula: C₇H₁₀N₄O

Molecular weight: 166.18

Ref: 4Z-T-8444

Thiamine Impurity 33

CAS: 1886-34-6

Formula: C₇H₁₀N₄O

Molecular weight: 166.18

Ref: ST-EA-CP-T2048

4-Amino-5-(formamidomethyl)-2-methylpyrimidine

Controlled Product

CAS: 1886-34-6

Stability Air Sensitive, Light Sensitive
Applications 4-Amino-5-(formamidomethyl)-2-methylpyrimidine is a metabolite of thiamine (T344185), a essential nutrient required for carbohydrate metabolism; also involved in nerve function.
References Kawaski, T., et al.: Methods Enzymol., 122, 15 (1986), Mascher, H., et al.: J. Pharm. Sci., 82, 56 (1993),

Formula: C₇H₁₀N₄O

Color and Shape: Off-White To Light Yellow

Molecular weight: 166.18

Ref: TR-A609675

2-Methyl-4-amino-5-(formylaminomethyl)pyrimidine

CAS: 1886-34-6

2-Methyl-4-amino-5-(formylaminomethyl)pyrimidine is a fine chemical that is used as a building block in the synthesis of other compounds. It is also known to be a reagent and speciality chemical. This substance has been shown to be an intermediate in the production of certain drugs, such as cefalotin, a penicillin antibiotic. 2-Methyl-4-amino-5-(formylaminomethyl)pyrimidine can be used as a versatile building block for the synthesis of many different compounds. It can also be used as an intermediate for the manufacture of other substances, such as antibiotics and dyes.

Formula: C₇H₁₀N₄O

Purity: Min. 91.0 Area-%

Molecular weight: 166.19 g/mol

Ref: 3D-J-400309

N-[(4-Amino-2-methylpyrimidin-5-yl)methyl]formamide

CAS: 1886-34-6

N-[(4-Amino-2-methylpyrimidin-5-yl)methyl]formamide (NAMPT) is a triazolo compound that inhibits the ATP binding cassette transporter and blocks the uptake of uridine and pyrimidine compounds. It also inhibits inorganic pyrophosphatase, which is an enzyme that catalyzes the hydrolysis of pyrophosphate to inorganic phosphate. NAMPT has been shown to be a substrate for hypochlorous acid production in neutrophils, suggesting it may play a role in the regulation of oxidative stress. Chemical biology studies have demonstrated that NAMPT plays a physiological function as an intermediate in vitamin B1 biosynthesis.

Formula: C₇H₁₀N₄O

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 166.18 g/mol

Ref: 3D-FA31702