2,2-diureidoacetic acid 2,2-二脲基乙酸
CAS 99-16-1 MFCD00007949
化学结构图
SMILES: NC(=O)NC(NC(N)=O)C(=O)O
化学属性
| Mol. Formula | C4 H8 N4 O4 |
|---|---|
| Mol. Weight | 176.13 |
| Melting Point | 154-156°C (dec.) |
| Boiling Point | |
| Flash Point | - |
别名和识别编码
| Chemical Name | 2,2-diureidoacetic acid |
|---|---|
| CAS Number | 99-16-1 |
| Synonym | 2,2-Bis(carbamoylamino)acetic acid 2,2-Bis[(aminocarbonyl)amino]acetic Acid Acetic acid, bis[(aminocarbonyl)amino]- Allantoic Acid {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} { {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} { |
| MDL Number | - |
| PubChem Substance ID | 203 |
| EC Number | 202-735-4 |
| Chemical Name Translation | 2,2-二脲基乙酸 |
| InChIKey | NUCLJNSWZCHRKL-UHFFFAOYSA-N |
| InChI | InChI=1S/C4H8N4O4/c5-3(11)7-1(2(9)10)8-4(6)12/h1H,(H,9,10)(H3,5,7,11)(H3,6,8,12) |
| Canonical SMILES | - |
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分类
- Metabolites & Impurities
- {uni_hamburg} no charge; urea; carboxylic acid; 1fragment
- {SA} Building Blocks, C1 to C5, Carbonyl Compounds, Carboxylic Acids, Chemical Synthesis, Metabolic Pathways, Metabolites and Cofactors on the Metabolic Pathways Chart, Metabolomics, Nucleotide, Organic Building Blocks
产品应用
- An metabolic intermediate in nucleic acid metabolism.
相关文献及参考
- [2]. Okumura I, et, al. Stereospecificity of conversion of uric acid into allantoic acid by enzymes of Canadida utilis. J Biochem. 1976 May;79(5):1013-9.
- [3]. Cai HL, et, al. Therapeutic efficacy of atypical antipsychotic drugs by targeting multiple stress-related metabolic pathways. Transl Psychiatry. 2017 May 16; 7(5):e1130.
- Short: EINECS Title: EINECS (European Inventory of Existing Commercial Chemical Substances) Source: Official Journal of the European Communities Volume: C 146 A (15.06.1990) Page: 1 Year: 1990 Internet Resource: http://ecb.jrc.ec.europa.eu/esis/index.php?PGM=ein Publish_Date: 1990/06/15
- Short: III/39 Title: Nuclear Quadrupole Resonance Spectroscopy Data Author: Chihara, H.; Nakamura, N. Editor: Chihara, H. Source: Landolt-Börnstein, New Series Volume: III/39 Year: 1997 Keyword: NQR; spectroscopy ISBN: 3-540-62428-7 ISBN: 978-3-540-62428-8 Internet Resource: DOI:10.1007/b61951 RefComment: VIII, 424 pages. Hardcover A
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