6275-84-9 Usage
Uses
Used in Medical Applications:
2,4-DIOXO-1-PHENYL-1,2,3,4-TETRAHYDRO-5-PYRIMIDINECARBONITRILE is used as a diuretic for the treatment of conditions such as congestive heart failure, liver disease, and kidney disorders. It helps in reducing fluid retention in the body by increasing urine production, thereby alleviating symptoms associated with these conditions.
Used in Congestive Heart Failure Treatment:
In the medical industry, 2,4-DIOXO-1-PHENYL-1,2,3,4-TETRAHYDRO-5-PYRIMIDINECARBONITRILE is used as a diuretic to manage congestive heart failure. It helps in reducing the workload on the heart by decreasing fluid buildup and improving the pumping efficiency of the heart.
Used in Liver Disease Management:
2,4-DIOXO-1-PHENYL-1,2,3,4-TETRAHYDRO-5-PYRIMIDINECARBONITRILE is used as a diuretic in the treatment of liver disease to help manage fluid retention and reduce the strain on the liver.
Used in Kidney Disorder Treatment:
In the medical industry, 2,4-DIOXO-1-PHENYL-1,2,3,4-TETRAHYDRO-5-PYRIMIDINECARBONITRILE is used as a diuretic for the management of kidney disorders. It aids in enhancing urine production, which helps in the removal of excess fluid and waste products from the body, thus supporting kidney function.
Used in Oral and Intravenous Administration:
2,4-DIOXO-1-PHENYL-1,2,3,4-TETRAHYDRO-5-PYRIMIDINECARBONITRILE is used in both oral and intravenous forms for medical use, allowing for flexible administration options based on the patient's condition and healthcare professional's recommendations.
Check Digit Verification of cas no
The CAS Registry Mumber 6275-84-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,7 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6275-84:
(6*6)+(5*2)+(4*7)+(3*5)+(2*8)+(1*4)=109
109 % 10 = 9
So 6275-84-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H7N3O2/c12-6-8-7-14(11(16)13-10(8)15)9-4-2-1-3-5-9/h1-5,7H,(H,13,15,16)
6275-84-9Relevant academic research and scientific papers
A multi-component reaction to 5-cyanouracils: Synthesis and mechanistic study
Zhuang, Bo-Ren,Hsu, Gien-Jow,Sung, Kuangsen
, p. 3399 - 3404 (2007/10/03)
Acetonitrile as a solvent, excess of primary amines as general bases, and a reflux condition make the multi-component reactions of (2-cyanoacetyl) carbamate 1, ethyl orthoformate, and primary amines form 5-cyanouracils 4a-c feasibly. Mechanistic studies o
Synthesis of 1-Substituted 5-Cyanouracils
Wolfbeis, Otto S.
, p. 182 - 185 (2007/10/02)
Condensation of (cyanoacetyl)urea (1) with aniline and trimethoxymethane affords (3-anilino-2-cyanoacryloyl)urea (2a), which thermally cyclizes to form strongly fluorescent 5-cyano-1-phenyluracil (3a).By using 2-aminopyridine or trimethoxymethane, other u
