non-1-en-3-yl acetate
group of stereoisomers with the chemical formula C₁₁H₂₀O₂
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Summary
non-1-en-3-yl acetate is a group of stereoisomers[1].
Key Facts
- non-1-en-3-yl acetate's instance of is recorded as group of stereoisomers[2].
- non-1-en-3-yl acetate's CAS Registry Number is recorded as 31795-37-6[3].
- non-1-en-3-yl acetate's canonical SMILES is recorded as O=C(OC(C=C)CCCCCC)C[4].
- non-1-en-3-yl acetate's InChI is recorded as InChI=1S/C11H20O2/c1-4-6-7-8-9-11(5-2)13-10(3)12/h5,11H,2,4,6-9H2,1,3H3[5].
- non-1-en-3-yl acetate's InChIKey is recorded as PUWRLDPHAKKTKR-UHFFFAOYSA-N[6].
- non-1-en-3-yl acetate's chemical formula is recorded as C₁₁H₂₀O₂[7].
- non-1-en-3-yl acetate's subclass of is recorded as biogenic acyclic ester[8].
- non-1-en-3-yl acetate's PubChem CID is recorded as 169364[9].
- non-1-en-3-yl acetate's ChEBI ID is recorded as 172068[10].
- non-1-en-3-yl acetate's found in taxon is recorded as Thymus zygioides[11].
- non-1-en-3-yl acetate's Human Metabolome Database ID is recorded as HMDB0037106[12].
- non-1-en-3-yl acetate's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+184.14632988'}[13].
- non-1-en-3-yl acetate's SureChEMBL ID is recorded as 8152281[14].
- non-1-en-3-yl acetate's DSSTox substance ID is recorded as DTXSID10276592[15].
- non-1-en-3-yl acetate's DSSTox substance ID is recorded as DTXSID60885517[16].
- non-1-en-3-yl acetate's UniChem compound ID is recorded as 24498714[17].