Callicarpenal
0 sources
Callicarpenal
Summary
Callicarpenal is a type of chemical entity[1]. Callicarpenal ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (7 views/month).[2]
Key Facts
- Callicarpenal's instance of is recorded as type of chemical entity[3].
- Callicarpenal's chemical structure is recorded as Callicarpenal.svg[4].
- Callicarpenal's CAS Registry Number is recorded as 161105-12-0[5].
- Callicarpenal's canonical SMILES is recorded as CC1CCC2(C(C1(C)CC=O)CCC=C2C)C[6].
- Callicarpenal's InChI is recorded as InChI=1S/C16H26O/c1-12-6-5-7-14-15(12,3)9-8-13(2)16(14,4)10-11-17/h6,11,13-14H,5,7-10H2,1-4H3/t13-,14+,15+,16+/m1/s1[7].
- Callicarpenal's InChIKey is recorded as MPWIIQYWQOBNKS-UGUYLWEFSA-N[8].
- Callicarpenal's chemical formula is recorded as C₁₆H₂₆O[9].
- Callicarpenal's subclass of is recorded as aldehydes[10].
- Callicarpenal's ChEMBL ID is recorded as CHEMBL2229006[11].
- Callicarpenal's Freebase ID is recorded as /m/0n4bzsl[12].
- Callicarpenal's UNII is recorded as HX4WCL7DPK[13].
- Callicarpenal's ChemSpider ID is recorded as 9282422[14].
- Callicarpenal's PubChem CID is recorded as 11107286[15].
- Callicarpenal's ChEBI ID is recorded as 166993[16].
- Callicarpenal's found in taxon is recorded as Callicarpa americana[17].
- Callicarpenal's found in taxon is recorded as Callicarpa japonica[18].
- Callicarpenal's isomeric SMILES is recorded as C[C@@H]1CC[C@@]2(C@@HCCC=C2C)CC@@HCCC=C2C)C">[19].
- Callicarpenal's mass is recorded as {'unit': 'Q483261', 'amount': '+234.198365'}[20].
- Callicarpenal's SureChEMBL ID is recorded as 3677724[21].
- Callicarpenal's DSSTox substance ID is recorded as DTXSID00455470[22].
- Callicarpenal's Microsoft Academic ID is recorded as 2779273841[23].
- Callicarpenal's DSSTOX compound identifier is recorded as DTXCID40406289[24].
- Callicarpenal's UniChem compound ID is recorded as 33997706[25].
Why It Matters
Callicarpenal ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (7 views/month).[2]