Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C15H21NO |
| Molecular Weight | 231.3333 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCNC(CC)C(=O)C1=CC2=C(CCC2)C=C1
InChI
InChIKey=VJXZPPKMTRTYIH-UHFFFAOYSA-N
InChI=1S/C15H21NO/c1-3-14(16-4-2)15(17)13-9-8-11-6-5-7-12(11)10-13/h8-10,14,16H,3-7H2,1-2H3
| Molecular Formula | C15H21NO |
| Molecular Weight | 231.3333 |
| 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 23:11:46 GMT 2025
by
admin
on
Mon Mar 31 23:11:46 GMT 2025
|
| Record UNII |
R7AVR79ZV4
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
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Common Name | English | ||
|
Preferred Name | English | ||
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Systematic Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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WIKIPEDIA |
Designer-drugs-Indanyl-N-ethylbuphedrone
Created by
admin on Mon Mar 31 23:11:46 GMT 2025 , Edited by admin on Mon Mar 31 23:11:46 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
1487882-12-1
Created by
admin on Mon Mar 31 23:11:46 GMT 2025 , Edited by admin on Mon Mar 31 23:11:46 GMT 2025
|
PRIMARY | |||
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INDANYL-N-ETHYLBUPHEDRONE
Created by
admin on Mon Mar 31 23:11:46 GMT 2025 , Edited by admin on Mon Mar 31 23:11:46 GMT 2025
|
PRIMARY | Three 25-NBOMe-type drugs, three other phenethylamine-type drugs (25I-NBMD, RH34, and escaline), eight cathinone derivatives, and a phencyclidine analog MMXE, newly identified in ingredients of drug products before they were sold on the drugmarket | ||
|
112477320
Created by
admin on Mon Mar 31 23:11:46 GMT 2025 , Edited by admin on Mon Mar 31 23:11:46 GMT 2025
|
PRIMARY | |||
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R7AVR79ZV4
Created by
admin on Mon Mar 31 23:11:46 GMT 2025 , Edited by admin on Mon Mar 31 23:11:46 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |
