2-Phenyl-1,3-thiazole-5-carbaldehyde, with the CAS number 1011-40-1, is an organic compound characterized by its thiazole ring, which is a five-membered heterocyclic structure containing both sulfur and nitrogen atoms. This compound features a phenyl group attached to the thiazole, enhancing its aromatic properties. The presence of a formyl group (-CHO) at the 5-position of the thiazole ring contributes to its reactivity, making it a useful intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. 2-Phenyl-1,3-thiazole-5-carbaldehyde is typically a yellow to brown solid, and it is soluble in organic solvents such as ethanol and dichloromethane. Its chemical properties include the ability to undergo various reactions, including nucleophilic additions and condensation reactions, due to the electrophilic nature of the aldehyde group. Additionally, this compound may exhibit biological activity, which has been the subject of research in medicinal chemistry. Overall, its unique structure and functional groups make it a valuable compound in synthetic organic chemistry.

2-PHENYL-1,3-THIAZOLE-5-CARBALDEHYDE

1011-40-1: 2-Phenyl-1,3-thiazole-5-carboxaldehyde, 2-Phenyl-5-thiazolecarboxaldehyde, 2-Phenyl-Thiazole-5-Carbaldehyde, 2-Phenylthiazole-5-Carbaldehyde, 95+%, 2-Phenylthiazole-5-carbaldehyde, 2-Phenylthiazole-5-carboxaldehyde, 5-Thiazolecarboxaldehyde, 2-phenyl-, Chembrdg-Bb 4301192

5-Thiazolecarboxaldehyde, 2-phenyl-

2-Phenyl-1,3-thiazole-5-carbaldehyde

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CAS 1011-40-1: 2-PHENYL-1,3-THIAZOLE-5-CARBALDEHYDE

5-Thiazolecarboxaldehyde, 2-phenyl-

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