2-Oxoimidazolidine-4-carboxylic Acid - CAS 21277-16-7
Catalog: |
BB016744 |
Product Name: |
2-Oxoimidazolidine-4-carboxylic Acid |
CAS: |
21277-16-7 |
Synonyms: |
2-oxo-4-imidazolidinecarboxylic acid; 2-oxoimidazolidine-4-carboxylic acid |
IUPAC Name: | 2-oxoimidazolidine-4-carboxylic acid |
Description: | 2-Oxoimidazolidine-4-carboxylic Acid (CAS# 21277-16-7) is a useful research chemical. |
Molecular Weight: | 130.10 |
Molecular Formula: | C4H6N2O3 |
Canonical SMILES: | C1C(NC(=O)N1)C(=O)O |
InChI: | InChI=1S/C4H6N2O3/c7-3(8)2-1-5-4(9)6-2/h2H,1H2,(H,7,8)(H2,5,6,9) |
InChI Key: | KZKRPYCBSZIQKN-UHFFFAOYSA-N |
MDL: | MFCD00005258 |
LogP: | -1.27880 |
GHS Hazard Statement: | H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation] |
Precautionary Statement: | P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
WO-2021175200-A1 | Ferroptosis inhibitorsâ€"diarylamine para-acetamides | 20200302 |
WO-2021009083-A1 | Process for treating keratin fibers, combining a composition comprising a water-soluble silicate and a composition comprising an amino acid and/or an oligopeptide | 20190718 |
CN-109251207-A | The method of stereoselective syntheses asymmetric lactone | 20180929 |
WO-2019081303-A1 | SUBSTITUTED TRIAZOLE DERIVATIVES AND USES THEREOF | 20171024 |
CA-3084421-A1 | Substituted triazole derivatives and uses thereof | 20171024 |
PMID | Publication Date | Title | Journal |
21539809 | 20110617 | Glutathione is a physiologic reservoir of neuronal glutamate | Biochemical and biophysical research communications |
18452022 | 20080521 | Synthesis of imidazolidin-2-one-4-carboxylate and of (tetrahydro)pyrimidin-2-one-5-carboxylate via an efficient modification of the Hofmann rearrangement | Organic & biomolecular chemistry |
16440984 | 20060101 | New AZT conjugates as potent anti-HIV agents | Nucleosides, nucleotides & nucleic acids |
15501035 | 20041206 | Novel 2-oxoimidazolidine-4-carboxylic acid derivatives as hepatitis C virus NS3-4A serine protease inhibitors: synthesis, activity, and X-ray crystal structure of an enzyme inhibitor complex | Bioorganic & medicinal chemistry letters |
Complexity: | 156 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 130.03784206 |
Formal Charge: | 0 |
Heavy Atom Count: | 9 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 3 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 130.03784206 |
Rotatable Bond Count: | 1 |
Topological Polar Surface Area: | 78.4 Å2 |
Undefined Atom Stereocenter Count: | 1 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | -1.2 |
Online Inquiry
Customer Support
Customer Centered
Related Functional Groups
Carbonyl Compounds
Customers Also Viewed
INDUSTRY LEADERS TRUST OUR PRODUCTS