3. Structures
3.1 2D structure
3.2 3D structure
-1
-2
-3
23 23 0 1 0 0 0 0 0999 V2000
-1.3306 -0.9277 -1.6504 O 0 0 0 0 0 0 0 0 0 0 0 0
-0.0702 -1.4897 1.3444 O 0 0 0 0 0 0 0 0 0 0 0 0
-2.9347 -1.4392 -0.1297 O 0 0 0 0 0 0 0 0 0 0 0 0
3.9919 -0.4426 -0.5654 O 0 0 0 0 0 0 0 0 0 0 0 0
0.2524 0.6635 0.5021 N 0 0 0 0 0 0 0 0 0 0 0 0
-3.4354 1.2489 0.1842 N 0 0 0 0 0 0 0 0 0 0 0 0
1.9523 -0.9661 0.3936 N 0 0 0 0 0 0 0 0 0 0 0 0
-1.0884 1.1017 0.8720 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.0979 0.8495 -0.2487 C 0 0 1 0 0 0 0 0 0 0 0 0
0.6456 -0.6524 0.7908 C 0 0 0 0 0 0 0 0 0 0 0 0
1.1019 1.5531 -0.1227 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.1856 -0.6163 -0.6394 C 0 0 0 0 0 0 0 0 0 0 0 0
2.3446 1.2394 -0.4953 C 0 0 0 0 0 0 0 0 0 0 0 0
2.8541 -0.1221 -0.2355 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.3904 0.5564 1.7759 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.0586 2.1653 1.1419 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.8373 1.4310 -1.1411 H 0 0 0 0 0 0 0 0 0 0 0 0
0.7086 2.5469 -0.3082 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.0858 1.1742 -0.5974 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.4287 2.2321 0.4534 H 0 0 0 0 0 0 0 0 0 0 0 0
2.2704 -1.9116 0.5874 H 0 0 0 0 0 0 0 0 0 0 0 0
2.9937 1.9542 -0.9859 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.3921 -1.8739 -1.9019 H 0 0 0 0 0 0 0 0 0 0 0 0
1 12 1 0 0 0 0
1 23 1 0 0 0 0
2 10 2 0 0 0 0
3 12 2 0 0 0 0
4 14 2 0 0 0 0
5 8 1 0 0 0 0
5 10 1 0 0 0 0
5 11 1 0 0 0 0
6 9 1 0 0 0 0
6 19 1 0 0 0 0
6 20 1 0 0 0 0
7 10 1 0 0 0 0
7 14 1 0 0 0 0
7 21 1 0 0 0 0
8 9 1 0 0 0 0
8 15 1 0 0 0 0
8 16 1 0 0 0 0
9 12 1 0 0 0 0
9 17 1 0 0 0 0
11 13 2 0 0 0 0
11 18 1 0 0 0 0
13 14 1 0 0 0 0
13 22 1 0 0 0 0
4. International Nomenclature & Identifiers
4.1 IUPAC Name
(2S)-2-amino-3-(2,4-dioxopyrimidin-1-yl)propanoic acid
4.2 InChI
InChI=1S/C7H9N3O4/c8-4(6(12)13)3-10-2-1-5(11)9-7(10)14/h1-2,4H,3,8H2,(H,12,13)(H,9,11,14)/t4-/m0/s1
4.3 InChIKey
FACUYWPMDKTVFU-BYPYZUCNSA-N
4.4 Canonical SMILES
C1=CN(C(=O)NC1=O)CC(C(=O)O)N
4.5 Isomeric SMILES
C1=CN(C(=O)NC1=O)C[C@@H](C(=O)O)N
4.6 SDF file
5. Spectroscopic data
5.1 13C nuclear magnetic resonance (13C NMR)
5.2 1H nuclear magnetic resonance (1H NMR)
5.3 Mass spectrometry (MS)
5.4 Infrared spectroscopy (IR)
5.5 Ultraviolet/visible spectroscopy (UV/Vis)