3. Structures
3.1 2D structure
3.2 3D structure
-1
-2
-3
26 26 0 0 0 0 0 0 0999 V2000
2.1119 -0.0148 -0.4559 O 0 0 0 0 0 0 0 0 0 0 0 0
-0.1219 -2.4012 0.3229 O 0 0 0 0 0 0 0 0 0 0 0 0
-4.1178 -0.0139 -0.6897 O 0 0 0 0 0 0 0 0 0 0 0 0
1.7703 0.0022 1.8118 O 0 0 0 0 0 0 0 0 0 0 0 0
-0.0898 -0.0013 0.3124 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.7678 1.2045 0.1342 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.7653 -1.2115 0.1540 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.1214 1.2003 -0.2025 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.7970 -0.0097 -0.3609 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.1190 -1.2157 -0.1827 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.0703 2.5155 0.2969 C 0 0 0 0 0 0 0 0 0 0 0 0
1.3258 -0.0039 0.6656 C 0 0 0 0 0 0 0 0 0 0 0 0
3.5269 -0.0192 -0.2342 C 0 0 0 0 0 0 0 0 0 0 0 0
4.2356 -0.0313 -1.5718 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.6601 2.1341 -0.3442 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.6401 -2.1621 -0.3049 H 0 0 0 0 0 0 0 0 0 0 0 0
0.3370 2.6112 1.3088 H 0 0 0 0 0 0 0 0 0 0 0 0
0.7417 2.6114 -0.4314 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.7491 3.3610 0.1401 H 0 0 0 0 0 0 0 0 0 0 0 0
3.8103 0.8780 0.3271 H 0 0 0 0 0 0 0 0 0 0 0 0
3.8029 -0.9108 0.3395 H 0 0 0 0 0 0 0 0 0 0 0 0
5.3212 -0.0348 -1.4394 H 0 0 0 0 0 0 0 0 0 0 0 0
3.9472 -0.9136 -2.1526 H 0 0 0 0 0 0 0 0 0 0 0 0
3.9544 0.8453 -2.1647 H 0 0 0 0 0 0 0 0 0 0 0 0
0.8113 -2.2564 0.5476 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.4228 -0.9349 -0.7582 H 0 0 0 0 0 0 0 0 0 0 0 0
1 12 1 0 0 0 0
1 13 1 0 0 0 0
2 7 1 0 0 0 0
2 25 1 0 0 0 0
3 9 1 0 0 0 0
3 26 1 0 0 0 0
4 12 2 0 0 0 0
5 6 1 0 0 0 0
5 7 2 0 0 0 0
5 12 1 0 0 0 0
6 8 2 0 0 0 0
6 11 1 0 0 0 0
7 10 1 0 0 0 0
8 9 1 0 0 0 0
8 15 1 0 0 0 0
9 10 2 0 0 0 0
10 16 1 0 0 0 0
11 17 1 0 0 0 0
11 18 1 0 0 0 0
11 19 1 0 0 0 0
13 14 1 0 0 0 0
13 20 1 0 0 0 0
13 21 1 0 0 0 0
14 22 1 0 0 0 0
14 23 1 0 0 0 0
14 24 1 0 0 0 0
4. International Nomenclature & Identifiers
4.1 IUPAC Name
ethyl 2,4-dihydroxy-6-methylbenzoate
4.2 InChI
InChI=1S/C10H12O4/c1-3-14-10(13)9-6(2)4-7(11)5-8(9)12/h4-5,11-12H,3H2,1-2H3
4.3 InChIKey
UQSRXQMIXSZGLA-UHFFFAOYSA-N
4.4 Canonical SMILES
CCOC(=O)C1=C(C=C(C=C1C)O)O
4.5 Isomeric SMILES
-
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)