CAS 26032-72-4

2,4-dichloro-6-phenylpyrimidine

Description:

2,4-Dichloro-6-phenylpyrimidine is an organic compound characterized by its pyrimidine ring structure, which is a six-membered aromatic ring containing two nitrogen atoms at the 1 and 3 positions. The compound features two chlorine substituents at the 2 and 4 positions of the pyrimidine ring, contributing to its reactivity and potential applications in various chemical reactions. The presence of a phenyl group at the 6 position enhances its lipophilicity and may influence its biological activity. This compound is typically a solid at room temperature and is soluble in organic solvents. It is often utilized in the synthesis of pharmaceuticals and agrochemicals due to its ability to act as an intermediate in chemical reactions. Additionally, the dichloro and phenyl substituents can impart specific properties that may be beneficial in medicinal chemistry, such as enhancing potency or selectivity. Safety data should be consulted for handling, as halogenated compounds can pose environmental and health risks.

Formula: C₁₀H₆Cl₂N₂

InChI: InChI=1/C10H6Cl2N2/c11-9-6-8(13-10(12)14-9)7-4-2-1-3-5-7/h1-6H

SMILES: c1ccc(cc1)c1cc(Cl)nc(Cl)n1

2,4-Dichloro-6-phenylpyrimidine

CAS: 26032-72-4

Formula: C₁₀H₆Cl₂N₂

Purity: >98.0%(GC)

Color and Shape: White to Light yellow powder to crystal

Molecular weight: 225.07

Ref: 3B-D5505

Pyrimidine, 2,4-dichloro-6-phenyl-

CAS: 26032-72-4

Formula: C₁₀H₆Cl₂N₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 225.0740

Ref: IN-DA002RFU

2,4-Dichloro-6-phenylpyrimidine

CAS: 26032-72-4

2,4-Dichloro-6-phenylpyrimidine

Purity: 98%

Molecular weight: 225.08g/mol

Ref: 54-OR73705

2,4-Dichloro-6-phenylpyrimidine

CAS: 26032-72-4

Formula: C₁₀H₆Cl₂N₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 225.07

Ref: 10-F049497

2,4-Dichloro-6-phenylpyrimidine

CAS: 26032-72-4

2,4-Dichloro-6-phenylpyrimidine is a nucleophilic reagent that has been used to synthesize pyrimidine derivatives. It has been shown to react with cyanoacetic acid and malononitrile in the presence of an organolithium reagent to form 2,6-dichloro-2,4-dihydroxypyrimidine. This compound reacts with chlorine gas to give 2,4-dichloro-6-(chloromethyl)pyrimidine. This reaction is regioselective and does not affect the other substituents on the ring. The reaction proceeds via a nucleophilic attack on the carbon atom adjacent to the nitrogen atom.

Formula: C₁₀H₆Cl₂N₂

Purity: Min. 95%

Molecular weight: 225.07 g/mol

Ref: 3D-BBA03272