Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C14H23NO2S |
| Molecular Weight | 269.403 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC(C)SC1=CC(OC)=C(CCN)C=C1OC
InChI
InChIKey=KSZHVRPGICAZOA-UHFFFAOYSA-N
InChI=1S/C14H23NO2S/c1-5-10(2)18-14-9-12(16-3)11(6-7-15)8-13(14)17-4/h8-10H,5-7,15H2,1-4H3
| Molecular Formula | C14H23NO2S |
| Molecular Weight | 269.403 |
| 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
Sat Dec 16 09:24:19 GMT 2023
by
admin
on
Sat Dec 16 09:24:19 GMT 2023
|
| Record UNII |
NLC3VH4KZM
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
WIKIPEDIA |
PiHKAL
Created by
admin on Sat Dec 16 09:24:19 GMT 2023 , Edited by admin on Sat Dec 16 09:24:19 GMT 2023
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
207740-32-7
Created by
admin on Sat Dec 16 09:24:19 GMT 2023 , Edited by admin on Sat Dec 16 09:24:19 GMT 2023
|
PRIMARY | |||
|
NLC3VH4KZM
Created by
admin on Sat Dec 16 09:24:19 GMT 2023 , Edited by admin on Sat Dec 16 09:24:19 GMT 2023
|
PRIMARY | |||
|
44349798
Created by
admin on Sat Dec 16 09:24:19 GMT 2023 , Edited by admin on Sat Dec 16 09:24:19 GMT 2023
|
PRIMARY | |||
|
DTXSID20658365
Created by
admin on Sat Dec 16 09:24:19 GMT 2023 , Edited by admin on Sat Dec 16 09:24:19 GMT 2023
|
PRIMARY | |||
|
2C-T-17
Created by
admin on Sat Dec 16 09:24:19 GMT 2023 , Edited by admin on Sat Dec 16 09:24:19 GMT 2023
|
PRIMARY | 2C (2C-x) is a general name for the family of psychedelic phenethylamines containing methoxy groups on the 2 and 5 positions of a benzene ring. Most of these compounds also carry lipophilic substituents at the 4 position, usually resulting in more potent and more metabolically stable and longer acting compounds. Most of the currently known 2C compounds were first synthesized by Alexander Shulgin in the 1970s and 1980s, and published in his book, PiHKAL (Phenethylamines i Have Known And Loved). Dr. Shulgin also invented the term 2C, being an acronym for the 2 carbon atoms between the benzene ring and the amino group.[1] Shulgin, Alexander; Ann Shulgin (September 1991). PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press. ISBN 0-9630096-0-5. OCLC 25627628. |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
SALT/SOLVATE -> PARENT |
|
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |
|
