(±)-N-羟基-3,4-亚甲基双氧安非他命结构式
|
常用名 | (±)-N-羟基-3,4-亚甲基双氧安非他命 | 英文名 | (+/-)-n-hydroxy-3 4-methylenedioxyamphe& |
---|---|---|---|---|
CAS号 | 114562-59-3 | 分子量 | 195.21500 | |
密度 | N/A | 沸点 | N/A | |
分子式 | C10H13NO3 | 熔点 | N/A | |
MSDS | 中文版 美版 | 闪点 | N/A | |
符号 |
GHS07 |
信号词 | Warning |
中文名 | (±)-N-羟基-3,4-亚甲基双氧安非他命 |
---|---|
英文名 | 1-(1,3-Benzodioxol-5-yl)-N-hydroxy-2-propanamine |
分子式 | C10H13NO3 |
---|---|
分子量 | 195.21500 |
精确质量 | 195.09000 |
PSA | 50.72000 |
LogP | 1.71600 |
[Studies on the identification of psychotropic substances. IX. Preparation and various analytical data of reference standard of new psychotropic substances, N-ethyl methylenedioxyamphetamine, N-hydroxy methylenedioxyamphetamine, mecloqualone, 4-methylaminorex, phendimetrazine and phenmetrazine].
Eisei Shikenjo Hokoku. (111) , 66-74, (1993) The reference standards of N-Ethyl methylenedioxyamphetamine, N-Hydroxy methylenedioxy-amphetamine, Mecloqualone, 4-Methylaminorex. Phendimetrazine and Phenmetrazine were chemically prepared from comm... |
|
In vivo formation of aromatic hydroxylated metabolites of 3,4-(methylenedioxy)methamphetamine in the rat: identification by ion trap tandem mass spectrometric (MS/MS and MS/MS/MS) techniques.
Biol. Mass Spectrom. 20(11) , 677-86, (1991) Aromatic hydroxylation has been established as a pathway for the in vivo metabolism of 3,4-(methylenedioxy)methamphetamine (MDMA) in the rat. Hydroxylation occurred at positions 2, 5 and 6 of the 3,4-... |
|
Stimulus effects of N-monoethyl-1-(3,4-methylenedioxyphenyl)-2-aminopropane (MDE) and N-hydroxy-1-(3,4-methylenedioxyphenyl)-2-aminopropane (N-OH MDA) in rats trained to discriminate MDMA from saline.
Pharmacol. Biochem. Behav. 33(4) , 909-12, (1989) Tests of stimulus generalization were conducted using rats trained to discriminate 1.5 mg/kg of N-monomethyl-1-(3,4-methylenedioxyphenyl)-2-aminopropane HCl (MDMA) from saline in order to determine if... |