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
Approval Year
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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
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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
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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DTXSID901032534
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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PF0P8RBU0X
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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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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SUBSTANCE RECORD
