CAS 1193-76-6
:5-bromodihydro-24(1h3h)-pyrimidinedione
Description:
5-Bromodihydro-2,4(1H,3H)-pyrimidinedione, with the CAS number 1193-76-6, is a heterocyclic organic compound characterized by its pyrimidine ring structure, which is a six-membered ring containing two nitrogen atoms at positions 1 and 3. The presence of a bromine atom at the 5-position contributes to its reactivity and potential applications in various chemical reactions. This compound typically exhibits properties such as moderate solubility in polar solvents and may participate in hydrogen bonding due to the presence of carbonyl groups. Its structure suggests potential biological activity, making it of interest in medicinal chemistry and drug development. The compound may also serve as an intermediate in organic synthesis, particularly in the preparation of other nitrogen-containing heterocycles. Safety data should be consulted for handling, as halogenated compounds can pose health risks. Overall, 5-bromodihydro-2,4(1H,3H)-pyrimidinedione is a valuable compound in both research and industrial applications.
Formula:C4H5BrN2O2
InChI:InChI=1/C4H5BrN2O2/c5-2-1-6-4(9)7-3(2)8/h2H,1H2,(H2,6,7,8,9)/t2-/m1/s1
SMILES:C1[C@H](C(=NC(=N1)O)O)Br
Synonyms:- 5-Bromo-5,6-Dihydrouracil
- 5-bromodihydropyrimidine-2,4(1H,3H)-dione
- (5S)-5-bromodihydropyrimidine-2,4(1H,3H)-dione
- (5R)-5-bromodihydropyrimidine-2,4(1H,3H)-dione
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Found 3 products.
5-Bromodihydrouracil
CAS:Controlled ProductFormula:C4H5BrN2O2Color and Shape:NeatMolecular weight:192.9995-Bromodihydrouracil-13C1, 15N2
CAS:Controlled Product<p>Applications 5-Bromodihydrouracil-13C1, 15N2 is the isotope labelled analog of 5-Bromodihydrouracil. 5-Bromodihydrouracil is predominantly used as a research agent for dihydropyrimidinase and dihydropyrimidine dehydrogenase.<br>References Porter, D., et al.: J. Biol. Chem., 269 (24177); Kikugawa, M., et al.: Eur. J. Biochem, 219, 393 (1994)<br></p>Formula:C3CH5BrN2O2Color and Shape:NeatMolecular weight:195.98

