U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C13H16BrNO2
Molecular Weight 298.176
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3C-B-FLY

SMILES

CC(N)CC1=C2OCCC2=C(Br)C3=C1CCO3

InChI

InChIKey=FKRREVSELFOLDT-UHFFFAOYSA-N
InChI=1S/C13H16BrNO2/c1-7(15)6-10-8-2-4-17-13(8)11(14)9-3-5-16-12(9)10/h7H,2-6,15H2,1H3

HIDE SMILES / InChI

Molecular Formula C13H16BrNO2
Molecular Weight 298.176
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Comparison of the behavioral responses induced by phenylalkylamine hallucinogens and their tetrahydrobenzodifuran ("FLY") and benzodifuran ("DragonFLY") analogs.
2019-01
Substance Class Chemical
Created
by admin
on Wed Apr 02 12:15:32 GMT 2025
Edited
by admin
on Wed Apr 02 12:15:32 GMT 2025
Record UNII
7FBG8DMS2E
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1-(8-BROMO-2,3,6,7-TETRAHYDROBENZO(1,2-B:4,5-B')DIFURAN-4-YL)PROPAN-2-AMINE
Preferred Name English
3C-B-FLY
Common Name English
8-BROMO-2,3,6,7-TETRAHYDRO-.ALPHA.-METHYL-BENZO(1,2-B:4,5-B')DIFURAN-4-ETHANAMINE
Systematic Name English
BENZO(1,2-B:4,5-B')DIFURAN-4-ETHANAMINE, 8-BROMO-2,3,6,7-TETRAHYDRO-.ALPHA.-METHYL-
Systematic Name English
Code System Code Type Description
FDA UNII
7FBG8DMS2E
Created by admin on Wed Apr 02 12:15:32 GMT 2025 , Edited by admin on Wed Apr 02 12:15:32 GMT 2025
PRIMARY
PUBCHEM
10017554
Created by admin on Wed Apr 02 12:15:32 GMT 2025 , Edited by admin on Wed Apr 02 12:15:32 GMT 2025
PRIMARY
CAS
219986-75-1
Created by admin on Wed Apr 02 12:15:32 GMT 2025 , Edited by admin on Wed Apr 02 12:15:32 GMT 2025
PRIMARY
WIKIPEDIA
DOB-FLY
Created by admin on Wed Apr 02 12:15:32 GMT 2025 , Edited by admin on Wed Apr 02 12:15:32 GMT 2025
PRIMARY
EPA CompTox
DTXSID80434288
Created by admin on Wed Apr 02 12:15:32 GMT 2025 , Edited by admin on Wed Apr 02 12:15:32 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY