Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C18H20FN |
| Molecular Weight | 269.3565 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
FC1=CC=CC=C1C(CC2=CC=CC=C2)N3CCCC3
InChI
InChIKey=ZAGWVXYVNFPCLW-UHFFFAOYSA-N
InChI=1S/C18H20FN/c19-17-11-5-4-10-16(17)18(20-12-6-7-13-20)14-15-8-2-1-3-9-15/h1-5,8-11,18H,6-7,12-14H2
| Molecular Formula | C18H20FN |
| Molecular Weight | 269.3565 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:23:52 GMT 2025
by
admin
on
Mon Mar 31 23:23:52 GMT 2025
|
| Record UNII |
S8L5P832B3
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
Download
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Preferred Name | English | ||
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Common Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English |
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WIKIPEDIA |
Designer-drugs-Fluorolintane
Created by
admin on Mon Mar 31 23:23:52 GMT 2025 , Edited by admin on Mon Mar 31 23:23:52 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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S8L5P832B3
Created by
admin on Mon Mar 31 23:23:52 GMT 2025 , Edited by admin on Mon Mar 31 23:23:52 GMT 2025
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PRIMARY | |||
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FLUOROLINTANE
Created by
admin on Mon Mar 31 23:23:52 GMT 2025 , Edited by admin on Mon Mar 31 23:23:52 GMT 2025
|
PRIMARY | Fluorolintane (also known as 2-FPPP) is a dissociative anesthetic drug that has been sold online as a designer drug.Fluorolintane and related diarylethylamines are antagonists of the NMDA receptor[3] and have been studied in vitro as potential treatments for neurotoxic injury, depression and as sympathomimetic. | ||
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137332216
Created by
admin on Mon Mar 31 23:23:52 GMT 2025 , Edited by admin on Mon Mar 31 23:23:52 GMT 2025
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PRIMARY | |||
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2149042-90-8
Created by
admin on Mon Mar 31 23:23:52 GMT 2025 , Edited by admin on Mon Mar 31 23:23:52 GMT 2025
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PRIMARY |