Matches any text strings used to describe a molecule.
Systematic Name, Synonym, Trade Name, Registry Number, SMILES, InChI or CSID

Systematic names 1,2-dihydroxybenzene
Synonyms AIBN
Trade names Aspirin
Registry numbers 7732-18-5
SMILES O=C(OCC)C
InChl InChI=1/CH4/h1H4
Search Hits Limit:
Single/Multi-component
Isotopically Labeled
Additional Filters

Found 7 results

Search term: ONOVZUNPHDZFBJ (Found by InChIKey (skeleton match))
IDStructureMolecular FormulaMolecular Weight# of Data Sources# of References# of PubMed# of RSC
2130387

0 of 4 defined stereocentres - 0/4 defined
InChI=1/C20H26O6/c1-5-25-18(22)16-14(21)11-20(4,24)17(19(23)26-6-2)15(16)13-9-7-12(3)8-10-13/h7-10,15-17,24H,5-6,11H2,1-4H3
C20H26O6362.4168421900
5441670

4 of 4 defined stereocentres - 4/4 defined
InChI=1/C20H26O6/c1-5-25-18(22)16-14(21)11-20(4,24)17(19(23)26-6-2)15(16)13-9-7-12(3)8-10-13/h7-10,15-17,24H,5-6,11H2,1-4H3/t15-,16-,17+,20-/m0/s1
C20H26O6362.41682100
5441671

4 of 4 defined stereocentres - 4/4 defined
InChI=1/C20H26O6/c1-5-25-18(22)16-14(21)11-20(4,24)17(19(23)26-6-2)15(16)13-9-7-12(3)8-10-13/h7-10,15-17,24H,5-6,11H2,1-4H3/t15-,16+,17+,20-/m0/s1
C20H26O6362.41682100
5441672

4 of 4 defined stereocentres - 4/4 defined
InChI=1/C20H26O6/c1-5-25-18(22)16-14(21)11-20(4,24)17(19(23)26-6-2)15(16)13-9-7-12(3)8-10-13/h7-10,15-17,24H,5-6,11H2,1-4H3/t15-,16+,17-,20+/m1/s1
C20H26O6362.41682100
5441673

4 of 4 defined stereocentres - 4/4 defined
InChI=1/C20H26O6/c1-5-25-18(22)16-14(21)11-20(4,24)17(19(23)26-6-2)15(16)13-9-7-12(3)8-10-13/h7-10,15-17,24H,5-6,11H2,1-4H3/t15-,16-,17-,20+/m1/s1
C20H26O6362.41682100
923967

4 of 4 defined stereocentres - 4/4 defined
InChI=1/C20H26O6/c1-5-25-18(22)16-14(21)11-20(4,24)17(19(23)26-6-2)15(16)13-9-7-12(3)8-10-13/h7-10,15-17,24H,5-6,11H2,1-4H3/t15-,16+,17-,20-/m1/s1
C20H26O6362.41682100
1132061

4 of 4 defined stereocentres - 4/4 defined
InChI=1/C20H26O6/c1-5-25-18(22)16-14(21)11-20(4,24)17(19(23)26-6-2)15(16)13-9-7-12(3)8-10-13/h7-10,15-17,24H,5-6,11H2,1-4H3/t15-,16+,17-,20-/m0/s1
C20H26O6362.41682100

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