CAS 87-39-8

Violuric acid

Description:

Violuric acid, with the CAS number 87-39-8, is an organic compound that belongs to the class of heterocyclic compounds. It is characterized by its structure, which includes a pyrimidine ring fused with a urea moiety. This compound typically appears as a yellowish crystalline solid and is known for its solubility in water and organic solvents. Violuric acid exhibits acidic properties due to the presence of carboxylic acid functional groups, allowing it to participate in various chemical reactions, including acid-base reactions. It is often used in dye chemistry and as an intermediate in the synthesis of other organic compounds. Additionally, violuric acid can form complexes with metal ions, which is of interest in coordination chemistry. Its unique structural features and reactivity make it a subject of study in both organic synthesis and materials science. Safety precautions should be taken when handling this compound, as with many organic chemicals, to avoid potential health hazards.

Formula: C₄H₃N₃O₄

InChI: InChI=1S/C4H3N3O4/c8-2-1(7-11)3(9)6-4(10)5-2/h11H,(H2,5,6,8,9,10)

InChI key: InChIKey=JMUJZTASUDOAGC-UHFFFAOYSA-N

SMILES: N(O)=C1C(=O)NC(=O)NC1=O

Synonyms:

• 2,4,5,6(1H,3H)-Pyrimidinetetrone,5-oxime
• 5-(Hydroxyimino)barbituric acid
• 5-Isonitrosobarbituric acid
• Alloxan,5-Oxime
• NSC 56338
• Violuric Acid Hydrate
• Violuric acid
• pyrimidine-2,4,5,6(1H,3H)-tetrone 5-oxime

Violuric acid

CAS: 87-39-8

Violuric acid

Purity: 97%

Molecular weight: 157.08g/mol

Ref: 54-OR1002121

Violuric acid

CAS: 87-39-8

Violuric acid, a redox mediator, ensures laccase retains high-redox potential in directed evolution assays.

Formula: C₄H₃N₃O₄

Color and Shape: White To Pale Yellow Crystalline Powder

Molecular weight: 157.08

Ref: TM-T40995

Violuric acid

CAS: 87-39-8

Violuric acid is a chemical compound that is used in biological treatment. It has a hydroxyl group and UV absorption, which makes it reactive. Violuric acid undergoes protonation and deprotonation to form an acid complex with water. The nitrogen atoms in violuric acid can react with the oxygen atoms of water molecules to form nitrous acid, which then reacts with hydrogen peroxide to form an oxidizing agent. Violuric acid is synthesized by chain reactions between organic acids and inorganic acids. Violuric acid has a redox potential of −0.35 volts, making it an excellent reducing agent for organic compounds. In organic chemistry, violuric acid is used as a reducing agent for esters or amides.

Formula: C₄H₃N₃O₄

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 157.08 g/mol

Ref: 3D-AAA08739

Violuric acid

CAS: 87-39-8

Purity: 97%

Molecular weight: 157.09

Ref: 10-F620058

Violuric Acid

Controlled Product

CAS: 87-39-8

Stability Hygroscopic
Applications Violuric Acid, can be used for the synthesis of some novel pyrimidines fused aza-heterocycles, having broad spectrum of pharmacological activities, such as 2-Methyloxazolo[5,4-d]pyrimidine-5,7(4H,6H)-dione (M324600).
References Abdou, W., et al.: Trends in Heterocyclic Chem., 10, 57 (2005);

Formula: C₄H₃N₃O₄

Color and Shape: Neat

Molecular weight: 157.08

Ref: TR-V634600