Cas no 933745-52-9 (4-methylpyrimidine-2-carbaldehyde)

4-methylpyrimidine-2-carbaldehyde structure
933745-52-9 structure
Product Name:4-methylpyrimidine-2-carbaldehyde
CAS No:933745-52-9
MF:C6H6N2O
MW:122.12464094162
MDL:MFCD10700213
CID:1982176
Update Time:2024-10-26

4-methylpyrimidine-2-carbaldehyde Chemical and Physical Properties

Names and Identifiers

    • 2-PYRIMIDINECARBOXALDEHYDE, 4-METHYL-
    • 4-Methyl-2-pyrimidinecarboxaldehyde
    • 4-Methylpyrimidine-2-carbaldehyde
    • 4-Methyl-2-pyrimidinecarboxaldehyde (ACI)
    • 4-methylpyrimidine-2-carbaldehyde
    • MDL: MFCD10700213
    • Inchi: 1S/C6H6N2O/c1-5-2-3-7-6(4-9)8-5/h2-4H,1H3
    • InChI Key: UBGSMHJOMIMVAW-UHFFFAOYSA-N
    • SMILES: O=CC1N=C(C)C=CN=1

4-methylpyrimidine-2-carbaldehyde Pricemore >>

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4-methylpyrimidine-2-carbaldehyde Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: Trifluoroacetic acid Solvents: Acetone ,  Water ;  overnight, 40 °C
1.2 Reagents: Sodium bicarbonate Solvents: Water ;  neutralized
Reference
Steric interference on the redox-conjugated pyrimidine ring rotation of mono- and dinuclear copper complexes with (4-methyl-2-pyrimidinyl)imine ligands
Hattori, Yohei; Nishikawa, Michihiro; Kusamoto, Tetsuro; Kume, Shoko; Nishihara, Hiroshi, Chemistry Letters, 2014, 43(7), 1037-1039

Production Method 2

Reaction Conditions
1.1 Reagents: Dimethyl sulfoxide ,  Oxalyl chloride Solvents: Dichloromethane ;  rt → -78 °C; 2 h, -78 °C
1.2 Reagents: Triethylamine ;  overnight, -78 °C → rt
1.3 Reagents: Water ;  1 h, rt
Reference
Pyrido[2,3-d]pyrimidin-4-one derivatives as tankyrase inhibitors and their preparation and use for the treatment of cancer
, World Intellectual Property Organization, , ,

Production Method 3

Reaction Conditions
Reference
Heteroaryl compounds as inhibitors of plasma kallikrein and their preparation
, World Intellectual Property Organization, , ,

4-methylpyrimidine-2-carbaldehyde Raw materials

4-methylpyrimidine-2-carbaldehyde Preparation Products

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