CAS 40261-59-4

Fórmula: C10H8N2O

InChI: InChI=1S/C10H8N2O/c13-8-9-6-7-12(11-9)10-4-2-1-3-5-10/h1-8H

Chave InChI: FDKVVJDPHDRHQS-UHFFFAOYSA-N

SMILES: C1=CC=C(C=C1)N2C=CC(=N2)C=O

1-Phenyl-1H-pyrazole-3-carbaldehyde

CAS: 40261-59-4

1-Phenyl-1H-pyrazole-3-carbaldehyde

Fórmula: C₁₀H₈N₂O

Pureza: 98%

Peso molecular: 172.18

Ref: 54-OR82422

1-Phenyl-1H-pyrazole-3-carbaldehyde

CAS: 40261-59-4

Fórmula: C₁₀H₈N₂O

Pureza: 98%

Cor e Forma: Solid

Peso molecular: 172.1833

Ref: IN-DA00CIYP

1-Phenyl-1H-pyrazole-3-carbaldehyde

CAS: 40261-59-4

1-Phenyl-1H-pyrazole-3-carbaldehyde

Fórmula: C₁₀H₈N₂O

Pureza: 95%

Peso molecular: 172.18

Ref: IN-DG221875

1-Phenyl-1H-pyrazole-3-carbaldehyde

CAS: 40261-59-4

Fórmula: C₁₀H₈N₂O

Pureza: 98%

Peso molecular: 172.187

Ref: 10-F336463

1-Phenyl-1H-pyrazole-3-carbaldehyde

CAS: 40261-59-4

1-Phenyl-1H-pyrazole-3-carbaldehyde is a pyrazole derivative that is used as a precursor in the synthesis of other compounds. The compound can be synthesized by nitro group reduction of 1,2,3-triazoles followed by chlorination of the resulting hydrazine. This reaction yields phenylhydrazones which undergo dehydrative condensation with carboxylic acids to give pyrazoles. These reactions are reversible and are catalyzed by acid or base. 1-Phenyl-1H-pyrazole-3-carbaldehyde has been shown to react with glucosyl residues in carbohydrates to form acetylated dihydroxyethyl moieties, which have been implicated in the prevention of diabetes and obesity.

Fórmula: C₁₀H₈N₂O

Pureza: Min. 95%

Peso molecular: 172.18 g/mol

Ref: 3D-QBA26159