IMPPAT Phytochemical information: 
(1R,4S,5R)-4-methoxy-4-methyl-1-propan-2-ylbicyclo[3.1.0]hexane

(1R,4S,5R)-4-methoxy-4-methyl-1-propan-2-ylbicyclo[3.1.0]hexane
Summary

IMPPAT Phytochemical identifier: IMPHY015562

Phytochemical name: (1R,4S,5R)-4-methoxy-4-methyl-1-propan-2-ylbicyclo[3.1.0]hexane

Synonymous chemical names:
cis-4-methoxythujane

External chemical identifiers:
CID:101850207
Chemical structure information

SMILES:
CO[C@@]1(C)CC[C@]2([C@H]1C2)C(C)C

InChI:
InChI=1S/C11H20O/c1-8(2)11-6-5-10(3,12-4)9(11)7-11/h8-9H,5-7H2,1-4H3/t9-,10-,11+/m0/s1

InChIKey:
SCWGDYORLGVQND-GARJFASQSA-N

DeepSMILES:
CO[C@@]C)CC[C@][C@H]5C3))CC)C

Functional groups:
COC
Molecular scaffolds

Scaffold Graph/Node/Bond level:
C1CC2CC2C1

Scaffold Graph/Node level:
C1CC2CC2C1

Scaffold Graph level:
C1CC2CC2C1
Chemical classification

ClassyFire Kingdom: Organic compounds

ClassyFire Superclass:
Lipids and lipid-like molecules

ClassyFire Class: Prenol lipids

ClassyFire Subclass: Monoterpenoids

NP Classifier Biosynthetic pathway: Terpenoids

NP Classifier Superclass: Monoterpenoids

NP Classifier Class: Thujane monoterpenoids

NP-Likeness score: 3.001


Chemical structure download