Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C14H23NO2 |
| Molecular Weight | 237.3379 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC(CC(C)N)=C(OC)C=C1C(C)C
InChI
InChIKey=SPKSLAUXKHSASF-UHFFFAOYSA-N
InChI=1S/C14H23NO2/c1-9(2)12-8-13(16-4)11(6-10(3)15)7-14(12)17-5/h7-10H,6,15H2,1-5H3
| Molecular Formula | C14H23NO2 |
| Molecular Weight | 237.3379 |
| 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 10:15:40 GMT 2023
by
admin
on
Sat Dec 16 10:15:40 GMT 2023
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| Record UNII |
PF0P8RBU0X
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| Record Status |
Validated (UNII)
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| Record Version |
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-
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WIKIPEDIA |
Designer-drugs-DOiPR
Created by
admin on Sat Dec 16 10:15:40 GMT 2023 , Edited by admin on Sat Dec 16 10:15:40 GMT 2023
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| Code System | Code | Type | Description | ||
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2,5-Dimethoxy-4-isopropylamphetamine
Created by
admin on Sat Dec 16 10:15:40 GMT 2023 , Edited by admin on Sat Dec 16 10:15:40 GMT 2023
|
PRIMARY | 2,5-Dimethoxy-4-isopropylamphetamine (also known as DOiP and DOiPr) is a psychedelic drug of the phenethylamine and amphetamine chemical classes.[1][2][3] It was first synthesized by Alexander Shulgin, and was described in his book PiHKAL (Phenethylamines i Have Known And Loved). Shulgin described DOiPR as being at least an order of magnitude weaker than DOPr, with doses of 20?30 mg required to produce valid changes in mental state.[4] Very little data exists about the pharmacological properties, metabolism, and toxicity of DOiPR. | ||
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42306-96-7
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DTXSID901032534
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PF0P8RBU0X
Created by
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44265275
Created by
admin on Sat Dec 16 10:15:40 GMT 2023 , Edited by admin on Sat Dec 16 10:15:40 GMT 2023
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