187305
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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关于此项目
线性分子式:
CH3OC6H4CH2CH2NH2
化学文摘社编号:
分子量:
151.21
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
200-245-5
Beilstein/REAXYS Number:
508967
MDL number:
产品名称
2-(4-甲氧苯基)乙胺, ≥98%
InChI key
LTPVSOCPYWDIFU-UHFFFAOYSA-N
InChI
1S/C9H13NO/c1-11-9-4-2-8(3-5-9)6-7-10/h2-5H,6-7,10H2,1H3
SMILES string
COc1ccc(CCN)cc1
assay
≥98%
form
liquid
refractive index
n20/D 1.538 (lit.)
bp
138-140 °C/20 mmHg (lit.)
254-256 °C
density
1.031 g/mL at 20 °C (lit.)
functional group
amine
Quality Level
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Application
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]
General description
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。
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
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)
The Pummerer cyclization route to the ibophyllidine alkaloids. Total synthesis of (?)-deethylibophyllidine.
Catena J, et al.
Tetrahedron Letters, 35(25), 4433-4436 (1994)
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
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
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)
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