CAS 4233-33-4

4-Phenyl-1,2,4-triazoline-3,5-dione

Description:

4-Phenyl-1,2,4-triazoline-3,5-dione, with the CAS number 4233-33-4, is a chemical compound characterized by its triazoline structure, which includes a five-membered ring containing three nitrogen atoms and two carbonyl groups. This compound typically appears as a crystalline solid and is known for its potential applications in organic synthesis and as a reagent in various chemical reactions. The presence of the phenyl group contributes to its aromatic properties, influencing its reactivity and stability. It is often utilized in the synthesis of other organic compounds due to its ability to participate in cycloaddition reactions and other transformations. Additionally, 4-Phenyl-1,2,4-triazoline-3,5-dione may exhibit interesting biological activities, although specific biological properties would require further investigation. As with many chemical substances, proper handling and safety precautions are essential, as it may pose hazards if not managed correctly.

Formula: C₈H₅N₃O₂

InChI: InChI=1S/C8H5N3O2/c12-7-9-10-8(13)11(7)6-4-2-1-3-5-6/h1-5H

InChI key: InChIKey=ISULLEUFOQSBGY-UHFFFAOYSA-N

SMILES: O=C1N(C(=O)N=N1)C2=CC=CC=C2

Synonyms:

• 3H-1,2,4-Triazole-3,5(4H)-dione, 4-phenyl-
• 4-Phenyl-1,2,4-Triazole-3,5-Dione
• 4-Phenyl-1,2,4-triazoline-3,5-dione
• 4-Phenyl-1,2,4-triazolinedione
• 4-Phenyl-3,5-dioxotriazole
• 4-Phenyl-3H-1,2,4-triazol-3,5(4H)-dion
• 4-Phenyl-3H-1,2,4-triazoline-3,5-dione
• 4-Phenyl-4,5-dihydro-3H-1,2,4-triazole-3,5-dione
• 4-Phenyl-4H-1,2,4-triazoline-3,5-dione
• 4-Phenyl-4H-[1,2,4]triazole-3,5-dione
• 4-Phenyl-Δ1-1,2,4-triazoline-3,5-dione
• 4-Phenyl-Δ¹-1,2,4-triazoline-3,5-dione
• 4-Phenyldehydrourazole
• 4-Phenyltriazoline-3,5-dione
• 4-fenil-3H-1,2,4-triazol-3,5(4H)-diona
• Azodicarboxylic acid N-phenylimide
• N-Phenyl-1,2,4-triazoline-3,5-dione
• N-Phenyl-1,3,4-triazoline-2,5-dione
• N-Phenyl-1,3,5-triazoline-2,4-dione
• N-Phenylazodicarboximide
• N-Phenylazodicarboxylic imide
• N-Phenyltriazoline-3,5-dione
• N-Phenyltriazolinedione
• Nsc 150362
• Ptad
• Triazole(4H-1,2,4)-3,5-Dione, 3,5-Dihydro-4-Phenyl-
• Δ1-1,2,4-Triazoline-3,5-dione, 4-phenyl-
• Δ¹-1,2,4-Triazoline-3,5-dione, 4-phenyl-

4-Phenyl-1,2,4-triazoline-3,5-dione

CAS: 4233-33-4

Formula: C₈H₅N₃O₂

Color and Shape: Red to Dark red to Dark purple powder to crystal

Molecular weight: 175.15

Ref: 3B-P1184

4-Phenyl-3H-1,2,4-triazole-3,5(4H)-dione

CAS: 4233-33-4

Formula: C₈H₅N₃O₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 175.1442

Ref: IN-DA00344V

4-Phenyl-1,2,4-triazoline-3,5-dione

CAS: 4233-33-4

4-Phenyl-1,2,4-triazoline-3,5-dione

Formula: C₈H₅N₃O₂

Purity: 95%

Color and Shape: purple solid

Molecular weight: 175.14g/mol

Ref: 54-OR939123

4-Phenyl-1,2,4-triazoline-3,5-dione

CAS: 4233-33-4

Applications Azodicarbonyl reagent used in the methods for determining levels of 1,25 dihydroxyvitamin d2 and d3 in biological and food samples and dietary supplements.
References Aranov, P. K. et al.: Anal. Bioanal. Chem., 391, 1917 ( 2008),

Formula: C₈H₅N₃O₂

Color and Shape: Neat

Molecular weight: 175.14

Ref: TR-P337380

4-Phenyl-3H-1,2,4-triazole-3,5(4H)-dione

CAS: 4233-33-4

Formula: C₈H₅N₃O₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 175.147

Ref: 10-F227815

4-Phenyl-1,2,3-triazoline-3,5-dione

CAS: 4233-33-4

4-Phenyl-1,2,3-triazoline-3,5-dione is a β-amino acid that is found in foods. It is produced by the cycloaddition process between a fatty acid and an α,β-unsaturated ketone. 4-Phenyl-1,2,3-triazoline-3,5-dione has been shown to have potential anticancer effects by inhibiting the production of prostaglandins (PGs) and thromboxanes (TXs). It has also been shown to inhibit the synthesis of tiglic acid in human serum.

Formula: C₈H₅N₃O₂

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 175.14 g/mol

Ref: 3D-FP26904