Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C17H25NO2 |
| Molecular Weight | 275.3859 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC2=C(OC=C2CCN(C(C)C)C(C)C)C=C1
InChI
InChIKey=NBFMSQBTYHYVKP-UHFFFAOYSA-N
InChI=1S/C17H25NO2/c1-12(2)18(13(3)4)9-8-14-11-20-17-7-6-15(19-5)10-16(14)17/h6-7,10-13H,8-9H2,1-5H3
| Molecular Formula | C17H25NO2 |
| Molecular Weight | 275.3859 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:08:25 GMT 2025
by
admin
on
Mon Mar 31 23:08:25 GMT 2025
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| Record UNII |
98H5PQ3THV
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| Record Status |
Validated (UNII)
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| Record Version |
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Download
| Name | Type | Language | ||
|---|---|---|---|---|
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Preferred Name | English | ||
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Common Name | English |
| Classification Tree | Code System | Code | ||
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WIKIPEDIA |
Designer-drugs-5-MeO-DiBF
Created by
admin on Mon Mar 31 23:08:25 GMT 2025 , Edited by admin on Mon Mar 31 23:08:25 GMT 2025
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| Code System | Code | Type | Description | ||
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5-MEO-DIBF
Created by
admin on Mon Mar 31 23:08:25 GMT 2025 , Edited by admin on Mon Mar 31 23:08:25 GMT 2025
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PRIMARY | 5-MeO-DiBF is a psychedelic[1] that has been sold online as a designer drug. It acts as an agonist for the 5-HT1A and 5-HT2 family of serotonin receptors. It is related in structure to the psychedelic tryptamine derivative 5-MeO-DiPT, but with the indole nitrogen replaced by oxygen, making 5-MeO-DiBF a benzofuran derivative. It is several times less potent as a serotonin agonist than 5-MeO-DiPT and with relatively more activity at 5-HT1A, but still shows strongest effects at the 5-HT2 family of receptors. | ||
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98H5PQ3THV
Created by
admin on Mon Mar 31 23:08:25 GMT 2025 , Edited by admin on Mon Mar 31 23:08:25 GMT 2025
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125276632
Created by
admin on Mon Mar 31 23:08:25 GMT 2025 , Edited by admin on Mon Mar 31 23:08:25 GMT 2025
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