2-ethylpyrimidine-4,6-diol

2-ethylpyrimidine-4,6-diol

(2S,3R)-3-(6-chloro-5-fluoropyrimidin-4-yl)-2-(2,4-difluorophenyl)butan-2-ol hydrochloride

(2S,3R)-3-(6-chloro-5-fluoropyrimidin-4-yl)-2-(2,4-difluorophenyl)butan-2-ol hydrochloride

2-(2-fluorophenyl)pyrimidine-5-carbaldehyde

$200.00
CAS No.: 946707-17-1
Catalog No.: 196462
Purity: 95%
MF: C11H7FN2O
MW: 202.188
Storage: 2-8 degree Celsius
SMILES: FC1=C(C=CC=C1)C1=NC=C(C=N1)C=O
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2-(2-fluorophenyl)pyrimidine-5-carbaldehyde; CAS No.: 946707-17-1; 2-(2-fluorophenyl)pyrimidine-5-carbaldehyde. PROPERTIES: 2-(2-fluorophenyl)pyrimidine-5-carbaldehyde features molecular formula C11H7FN2O with molecular weight approximately 204.18 g/mol. It generally appears as a pale yellow solid with a reported melting point of 98-101 C. The compound exhibits moderate solubility in polar organic solvents and limited water solubility. Proper storage involves keeping in a tightly sealed container at room temperature away from moisture and light. Safety precautions include using personal protective equipment during handling to prevent skin and eye contact, as it may cause irritation. The aldehyde group is reactive and may form complexes with metals. In case of accidental release, absorb with inert material and dispose of properly. APPLICATIONS: 2-(2-fluorophenyl)pyrimidine-5-carbaldehyde functions as a valuable intermediate in pharmaceutical synthesis. Its fluorophenyl substituent provides valuable steric and electronic effects for receptor binding. In medicinal chemistry, it has been employed in developing novel kinase inhibitors, as reported in oncology-focused pharmaceutical research journals. The carbaldehyde group enables formation of imine bonds for further structural elaboration. Additionally, this compound serves as a building block for specialty chemicals, with applications described in fine chemical literature focusing on heterocyclic compounds for material science.

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