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Merck
CN

187305

Sigma-Aldrich

2-(4-甲氧苯基)乙胺

≥98%

别名:

2-(4-甲氧苯基)乙胺, 4-甲氧基苯乙胺

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About This Item

线性分子式:
CH3OC6H4CH2CH2NH2
CAS号:
分子量:
151.21
Beilstein:
508967
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

≥98%

表单

liquid

折射率

n20/D 1.538 (lit.)

沸点

138-140 °C/20 mmHg (lit.)
254-256 °C

密度

1.031 g/mL at 20 °C (lit.)

官能团

amine

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。

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[(4-甲氧基苄氨基)聚磷腈和聚[(4-甲氧基苯乙基氨基)聚磷腈]

象形图

Corrosion

警示用语:

Danger

危险声明

危险分类

Skin Corr. 1B

储存分类代码

8A - Combustible corrosive hazardous materials

WGK

WGK 3

闪点(°F)

230.0 °F - closed cup

闪点(°C)

110 °C - closed cup

个人防护装备

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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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)
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
W J Keller et al.
Journal of pharmaceutical sciences, 65(10), 1539-1540 (1976-10-01)
It has been established that the oxidative deamination of tyramine by monoamine xodase is inhibited by (+/-)-4-methoxy-beta-hydroxyphenethylamine and its N-methylated derivatives. This particular series of compounds does not inhibit the action of monoamine oxidase when tryptamine is used as the
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)
The Pummerer cyclization route to the ibophyllidine alkaloids. Total synthesis of (?)-deethylibophyllidine.
Catena J, et al.
Tetrahedron Letters, 35(25), 4433-4436 (1994)

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