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Merck
CN

270229

Sigma-Aldrich

3-甲氧基苯乙胺

97%

别名:

2-(3-甲氧基苯基)乙胺

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About This Item

线性分子式:
CH3OC6H4CH2CH2NH2
CAS号:
分子量:
151.21
Beilstein:
775202
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

97%

表单

liquid

折射率

n20/D 1.538 (lit.)

沸点

118-119 °C/6 mmHg (lit.)

密度

1.038 g/mL at 25 °C (lit.)

官能团

amine

SMILES字符串

COc1cccc(CCN)c1

InChI

1S/C9H13NO/c1-11-9-4-2-3-8(7-9)5-6-10/h2-4,7H,5-6,10H2,1H3

InChI key

WJBMRZAHTUFBGE-UHFFFAOYSA-N

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一般描述

The spectral binding affinity for 3-methoxyphenethylamine was studied to examine the determinants of P450 2D6 catalysis.

应用

3-Methoxyphenethylamine was used in the perfluorooctanesulfonic acid catalyzed Pictet-Spengler reaction. It was also used in the synthesis of 1,3-oxazepines via palladium-catalyzed intramolecular coupling.

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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分析证书(COA)

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Tetrahedron Letters, 48, 835-835 (2007)
Tetrahedron, 62, 9002-9002 (2006)
P T Wong et al.
Neuroreport, 5(1), 53-56 (1993-10-25)
The effects of death and various treatments that affect the status of nigrostriatal neurones on striatal release of dopamine (DA) and 5-hydroxytryptamine (5-HT) and their metabolites 3,4-dihydroxyphenylacetic acid (DOPAC), 3-methoxy-4-hydroxyphenylethylamine (3-MT), homovanillic acid (HVA) and 5-hydroxyindoleacetic acid (5-HIAA) were studied
G P Miller et al.
Biochemistry, 40(47), 14215-14223 (2001-11-21)
Cytochrome P450 (P450) 2D6 oxidizes a wide variety of drugs typically at a distance of 5-7 A from a basic nitrogen on the substrate. To investigate the determinants of P450 2D6 catalysis, we analyzed the binding and oxidation of phenethylamine
Anita H Lewin et al.
Bioorganic & medicinal chemistry, 16(15), 7415-7423 (2008-07-08)
A cell line in which RD-HGA16 cells were stably transfected with the hTAAR 1 receptor was created and utilized to carry out a systematic evaluation of a series of beta-phenethylamines. Fair agreement was observed with data obtained for aryl and

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