Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C10H13NO3.ClH |
| Molecular Weight | 231.676 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CC(CC1=CC=C2OCOC2=C1)NO
InChI
InChIKey=DMBCJQVFXIKFJX-UHFFFAOYSA-N
InChI=1S/C10H13NO3.ClH/c1-7(11-12)4-8-2-3-9-10(5-8)14-6-13-9;/h2-3,5,7,11-12H,4,6H2,1H3;1H
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Determination of a new designer drug, N-hydroxy-3,4-methylenedioxymethamphetamine and its metabolites in rats using ultra-performance liquid chromatography-tandem mass spectrometry. | 2010-05-20 |
|
| Degradation of N-hydroxy-3,4-methylenedioxymethamphetamine in aqueous solution and its prevention. | 2009-12-15 |
|
| Comparative potencies of 3,4-methylenedioxymethamphetamine (MDMA) analogues as inhibitors of [3H]noradrenaline and [3H]5-HT transport in mammalian cell lines. | 2007-12 |
Patents
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74341-83-6
Created by
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R0H604RFC0
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PN 005
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DTXSID5048891
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13958
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60196328
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admin on Mon Mar 31 22:20:39 GMT 2025 , Edited by admin on Mon Mar 31 22:20:39 GMT 2025
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PARENT (SALT/SOLVATE)
SUBSTANCE RECORD