IMPPAT Phytochemical information: 
(1R)-1,8-dimethyl-4-prop-1-en-2-ylspiro[4.5]dec-8-ene

(1R)-1,8-dimethyl-4-prop-1-en-2-ylspiro[4.5]dec-8-ene
Summary

IMPPAT Phytochemical identifier: IMPHY004190

Phytochemical name: (1R)-1,8-dimethyl-4-prop-1-en-2-ylspiro[4.5]dec-8-ene

Synonymous chemical names:
beta-acoradiene

External chemical identifiers:
CID:5316209
Chemical structure information

SMILES:
CC1=CCC2(CC1)[C@H](C)CCC2C(=C)C

InChI:
InChI=1S/C15H24/c1-11(2)14-6-5-13(4)15(14)9-7-12(3)8-10-15/h7,13-14H,1,5-6,8-10H2,2-4H3/t13-,14?,15?/m1/s1

InChIKey:
DVBSKQAFCDJNSL-WLYUNCDWSA-N

DeepSMILES:
CC=CCCCC6))[C@H]C)CCC5C=C)C

Functional groups:
C=C(C)C, CC=C(C)C
Molecular scaffolds

Scaffold Graph/Node/Bond level:
C1=CCC2(CC1)CCCC2

Scaffold Graph/Node level:
C1CCC2(CC1)CCCC2

Scaffold Graph level:
C1CCC2(CC1)CCCC2
Chemical classification

ClassyFire Kingdom: Organic compounds

ClassyFire Superclass:
Hydrocarbons

ClassyFire Class: Unsaturated hydrocarbons

ClassyFire Subclass: Branched unsaturated hydrocarbons

NP Classifier Biosynthetic pathway: Terpenoids

NP Classifier Superclass: Sesquiterpenoids

NP Classifier Class: Acorane sesquiterpenoids

NP-Likeness score: 3.348


Chemical structure download