质量水平
检测方案
≥98%
形式
liquid
折射率
n20/D 1.538 (lit.)
bp
138-140 °C/20 mmHg (lit.)
254-256 °C
密度
1.031 g/mL at 20 °C (lit.)
SMILES字符串
COc1ccc(CCN)cc1
InChI
1S/C9H13NO/c1-11-9-4-2-8(3-5-9)6-7-10/h2-5H,6-7,10H2,1H3
InChI key
LTPVSOCPYWDIFU-UHFFFAOYSA-N
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一般描述
4-甲氧基苯乙胺抑制单胺氧化酶催化的酪胺和色胺的脱氨基作用。
4-甲氧基苯乙胺被用于通过烷基化反应合成其他有机化合物的前体。
4-甲氧基苯乙胺被用于通过烷基化反应合成其他有机化合物的前体。
应用
4-甲氧基苯乙胺用于合成以下物质：
- 吡咯并[3,2-c咔唑
- 固定硝化碱基和寡核苷酸所需的聚（4-甲氧基苯乙胺）
- 有机聚磷腈，例如聚[双（4-甲氧基苄氨基）聚磷腈和聚[双（4-甲氧基苯乙基氨基）聚磷腈]
警示用语：
Danger
危险声明
危险分类
Skin Corr. 1B
WGK
WGK 3
闪点(°F)
closed cup
闪点(°C)
closed cup
个人防护装备
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Synthesis and characterization of novel polyorganophosphazenes substituted with 4-methoxybenzylamine and 4-methoxyphenethylamine for in vitro release of indomethacin and 5-fluorouracil.
Gudasi KB, et al.
Reactive functional Polymers, 66(10), 1149-1157 (2006)
GC--MS analysis of N-(bromodimethoxybenzyl)-2-, 3-, and 4-methoxyphenethylamines: Inverse analogues of the psychoactive 25B-NBOMe drug
Almalki AJ, et al.
Forensic Chemistry, 21, 100277-100277 (2020)
Electrochemical Investigation of oligonucleotide-DNA hybridization on poly(4-methoxyphenethylamine).
Francielle B Silva et al.
International journal of molecular sciences, 9(7), 1173-1188 (2009-03-28)
This work describes the immobilization of purine and pyrimidine bases and immobilization/hybridization of synthetic oligonucleotides on graphite electrodes modified with poly(4-methoxyphenethylamine) produced in acid medium. The immobilization of adenine, guanine, cytosine and thymine on these modified electrodes was efficient, producing
T Kuramoto et al.
Journal of neuroscience research, 6(1), 37-48 (1981-01-01)
K+-sensitive liquid ion exchange electrode systems respond with a slow potential change to acetylcholine, choline, anticholinergic drugs, biogenic amines, and glutamic acid. The response threshold has been defined, and in most cases it is at extremely low concentrations (10(-7)-10(-5)M). The
F Peter Guengerich et al.
The Journal of biological chemistry, 277(37), 33711-33719 (2002-07-03)
Cytochrome P450 (P450) 2D6 is involved in the oxidation of a large fraction ( approximately 30%) of drugs used by humans and also catalyzes the O-demethylation of the model substrates 3- and 4-methoxyphenethylamine followed by subsequent ring hydroxylation to dopamine.
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