| Weight | 132.119 g/mol |
|---|---|
| Formula | C4H8N2O3 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 3 |
3-Ureidopropionic acid (462-88-4)
beta-ureidopropionic acid · N-carbamoyl-beta-alanine · ion(-1) of N-carbamoyl-beta-alanine
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- Sigma-Aldrich - 3-Ureidopropionic acid87.60 USD
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- The catabolism of C14-labeled uracil, dihydrouracil, and beta-ureidopropionic acid in rat liver slices. (Journal of Biological Chemistry, 1957)
- Regulation of N-carbamoyl-beta-alanine amidohydrolase, the terminal enzyme in pyrimidine catabolism, by ligand-induced change in polymerization. (Journal of Biological Chemistry, 1987)
- The catabolism of C14-labeled uracil, dihydrouracil, and beta-ureidopropionic acid in the intact rat. (Journal of Biological Chemistry, 1957)
- Organotin esters of 3-ureidopropionic acid. Crystal structure of triphenyltin(IV) 3-ureidopropionate, (C6H5)3SnOCO(CH2)2NHCONH2 (Journal of Organometallic Chemistry, 1991)
- Amino Acid Studies. Part II. Structure and Synthesis of Albizziine (L-2-Amino-3-ureidopropionic Acid), an Amino Acid from Higher Plants. (Acta Chemica Scandinavica, 1959)
- Pyridinyl compounds of N-carbamoyl-N-thiocarbamoyl- or N-amidino-glycine or beta-alanine useful as sweetening agents (1988)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - beta-ureidopropionic acid
- N-carbamoyl-beta-alanine
- ion(-1) of N-carbamoyl-beta-alanine
- beta-ureidopropionate
-
SMILESC(CNC(=O)N)C(=O)O
-
InChIKeyJSJWCHRYRHKBBW-UHFFFAOYSA-N
- Pubchem - 3-Ureidopropionic acid
- Wikipedia - N-carbamoyl-beta-alanine
3-Ureidopropionic acid, also called N-carbamoyl-beta-alanine, is an intermediate in the metabolism of uracil. It is a urea derivative of beta-alanine.
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Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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