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
Mon Mar 31 23:08:27 GMT 2025
by
admin
on
Mon Mar 31 23:08:27 GMT 2025
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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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-
Download
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Systematic Name | English | ||
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Preferred Name | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Systematic Name | English |
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WIKIPEDIA |
Designer-drugs-DOiPR
Created by
admin on Mon Mar 31 23:08:27 GMT 2025 , Edited by admin on Mon Mar 31 23:08:27 GMT 2025
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| Code System | Code | Type | Description | ||
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2,5-Dimethoxy-4-isopropylamphetamine
Created by
admin on Mon Mar 31 23:08:27 GMT 2025 , Edited by admin on Mon Mar 31 23:08:27 GMT 2025
|
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
admin on Mon Mar 31 23:08:27 GMT 2025 , Edited by admin on Mon Mar 31 23:08:27 GMT 2025
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44265275
Created by
admin on Mon Mar 31 23:08:27 GMT 2025 , Edited by admin on Mon Mar 31 23:08:27 GMT 2025
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