IMPPAT Phytochemical information: 
2-((3,3-Dimethyloxiran-2-yl)methyl)-3-methylfuran

2-((3,3-Dimethyloxiran-2-yl)methyl)-3-methylfuran
Summary

IMPPAT Phytochemical identifier: IMPHY009211

Phytochemical name: 2-((3,3-Dimethyloxiran-2-yl)methyl)-3-methylfuran

Synonymous chemical names:
rose furan epoxide, rosefuran epoxide, rosefurane epoxide, rosenfuran epoxide

External chemical identifiers:
CID:6428926
Chemical structure information

SMILES:
Cc1ccoc1CC1OC1(C)C

InChI:
InChI=1S/C10H14O2/c1-7-4-5-11-8(7)6-9-10(2,3)12-9/h4-5,9H,6H2,1-3H3

InChIKey:
BVTAIXWVSMPSFL-UHFFFAOYSA-N

DeepSMILES:
Ccccoc5CCOC3C)C

Functional groups:
CC1OC1(C)C, coc
Molecular scaffolds

Scaffold Graph/Node/Bond level:
c1coc(CC2CO2)c1

Scaffold Graph/Node level:
C1COC(CC2CO2)C1

Scaffold Graph level:
C1CCC(CC2CC2)C1
Chemical classification

ClassyFire Kingdom: Organic compounds

ClassyFire Superclass:
Organoheterocyclic compounds

ClassyFire Class: Heteroaromatic compounds

NP Classifier Biosynthetic pathway: Terpenoids

NP Classifier Superclass: Monoterpenoids

NP Classifier Class: Acyclic monoterpenoids

NP-Likeness score: 2.1


Chemical structure download