3-phenyl-2-thioxoimidazolidin-4-one-Imidazolidines| Ambeed

Chemistry Heterocyclic Building Blocks Imidazolidines 3-phenyl-2-thioxoimidazolidin-4-one

3-phenyl-2-thioxoimidazolidin-4-one

Ambeed provide 6 derivatives of 3-phenyl-2-thioxoimidazolidin-4-one.

These compounds have the same murcko framework: 3-phenyl-2-thioxoimidazolidin-4-one.

Nucleophilic Substitution: The thioxo group is susceptible to nucleophilic attack, and the compound can react with nucleophiles to form various products.
Acylation: The carbonyl group (C=O) can undergo acylation reactions with acylating agents (e.g., acyl halides or anhydrides) to form amides or other derivatives.
Reduction: The carbonyl group can be reduced to the corresponding alcohol using reducing agents such as lithium aluminum hydride (LiAlH₄) or sodium borohydride (NaBH₄).
Oxidation: The sulfur atom can be oxidized to form sulfoxides or sulfones.
Cyclization: Depending on the reaction conditions, the compound may undergo intramolecular cyclization reactions, forming different cyclic structures.
Reaction with Grignard Reagents: The compound can react with Grignard reagents to form new carbon-carbon bonds.
Halogenation: The phenyl group can be halogenated (e.g., chlorination or bromination) under appropriate conditions.
Substitution Reactions: The compound can undergo various substitution reactions, such as nucleophilic aromatic substitution or electrophilic aromatic substitution.

3-phenyl-2-thioxoimidazolidin-4-one

A1810814333-20-498%

$44.00/1g

A8890862010-15-398%

$94.00/1g

A5377244333-19-197%

$41.00/100mg

A6083774370-90-597%

$113.00/1g

A6218655624-27-195%

$76.00/250mg

A106429155180-53-397%

$604.00/1g