Details
Stereochemistry | RACEMIC |
Molecular Formula | C12H15NO |
Molecular Weight | 189.2536 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CNC(C)CC1=CC2=C(C=CO2)C=C1
InChI
InChIKey=QLAAURQYEAEHBO-UHFFFAOYSA-N
InChI=1S/C12H15NO/c1-9(13-2)7-10-3-4-11-5-6-14-12(11)8-10/h3-6,8-9,13H,7H2,1-2H3
Molecular Formula | C12H15NO |
Molecular Weight | 189.2536 |
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 11:25:40 GMT 2023
by
admin
on
Sat Dec 16 11:25:40 GMT 2023
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Record UNII |
4J6PD2FN87
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Record Status |
Validated (UNII)
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Record Version |
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-
Download
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Systematic Name | English |
Classification Tree | Code System | Code | ||
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WIKIPEDIA |
Designer-drugs-6-MAPB
Created by
admin on Sat Dec 16 11:25:40 GMT 2023 , Edited by admin on Sat Dec 16 11:25:40 GMT 2023
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Code System | Code | Type | Description | ||
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1354631-79-0
Created by
admin on Sat Dec 16 11:25:40 GMT 2023 , Edited by admin on Sat Dec 16 11:25:40 GMT 2023
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PRIMARY | |||
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122202866
Created by
admin on Sat Dec 16 11:25:40 GMT 2023 , Edited by admin on Sat Dec 16 11:25:40 GMT 2023
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PRIMARY | |||
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6-MAPB
Created by
admin on Sat Dec 16 11:25:40 GMT 2023 , Edited by admin on Sat Dec 16 11:25:40 GMT 2023
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PRIMARY | 6-MAPB (1-(benzofuran-6-yl)-N-methylpropan-2-amine) is a psychedelic and entactogenic drug which is structurally related to 6-APB and MDMA. It is not known to have been widely sold as a "designer drug" but has been detected in analytical samples taken from individuals hospitalised after using drug combinations that included other benzofuran derivatives. 6-MAPB was banned in the UK in June 2013, along with 9 other related compounds which were thought to produce similar effects. | ||
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4J6PD2FN87
Created by
admin on Sat Dec 16 11:25:40 GMT 2023 , Edited by admin on Sat Dec 16 11:25:40 GMT 2023
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PRIMARY | |||
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DTXSID301010102
Created by
admin on Sat Dec 16 11:25:40 GMT 2023 , Edited by admin on Sat Dec 16 11:25:40 GMT 2023
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PRIMARY |