α-terpinyl butyrate
pair of enantiomers
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α-terpinyl butyrate
Summary
α-terpinyl butyrate is a group of stereoisomers[1].
Key Facts
- α-terpinyl butyrate's instance of is recorded as group of stereoisomers[2].
- α-terpinyl butyrate's chemical structure is recorded as Alpha-Terpinyl butyrate.svg[3].
- α-terpinyl butyrate's CAS Registry Number is recorded as 2153-28-8[4].
- α-terpinyl butyrate's EC number is recorded as 218-445-6[5].
- α-terpinyl butyrate's canonical SMILES is recorded as CCCC(=O)OC(C)(C)C1CCC(=CC1)C[6].
- α-terpinyl butyrate's InChI is recorded as InChI=1S/C14H24O2/c1-5-6-13(15)16-14(3,4)12-9-7-11(2)8-10-12/h7,12H,5-6,8-10H2,1-4H3[7].
- α-terpinyl butyrate's InChIKey is recorded as LWKWNIYBQLKBMQ-UHFFFAOYSA-N[8].
- α-terpinyl butyrate's chemical formula is recorded as C₁₄H₂₄O₂[9].
- α-terpinyl butyrate's subclass of is recorded as chemical compound[10].
- α-terpinyl butyrate's UNII is recorded as L94B6AU40N[11].
- α-terpinyl butyrate's ChemSpider ID is recorded as 502793[12].
- α-terpinyl butyrate's PubChem CID is recorded as 578423[13].
- α-terpinyl butyrate's ChEBI ID is recorded as 171778[14].
- α-terpinyl butyrate's found in taxon is recorded as Scutellaria barbata[15].
- α-terpinyl butyrate's Human Metabolome Database ID is recorded as HMDB0032053[16].
- α-terpinyl butyrate's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+224.178'}[17].
- α-terpinyl butyrate's ECHA Substance Infocard ID is recorded as 100.016.769[18].
- α-terpinyl butyrate's SureChEMBL ID is recorded as 3504597[19].
- α-terpinyl butyrate's CosIng number is recorded as 40708[20].
- α-terpinyl butyrate's DSSTox substance ID is recorded as DTXSID30862850[21].
- α-terpinyl butyrate's JECFA database ID is recorded as 2492[22].
- α-terpinyl butyrate's DSSTOX compound identifier is recorded as DTXCID10811563[23].
- α-terpinyl butyrate's FL number is recorded as 09.052[24].
- α-terpinyl butyrate's JECFA number is recorded as 370[25].
- α-terpinyl butyrate's UniChem compound ID is recorded as 22752365[26].