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Merck
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文件

560448

Sigma-Aldrich

2,3-二甲氧基苯乙胺

97%

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About This Item

线性分子式:
(CH3O)2C6H3CH2CH2NH2
CAS号:
3213-29-4
分子量:
181.23
MDL號碼:
MFCD00060613
分類程式碼代碼:
12352100
PubChem物質ID:
24879865

化驗

97%

藥物控制

USDEA Schedule I

折射率

n20/D 1.5320 (lit.)

bp

261-262 °C (lit.)

密度

1.178 g/mL

SMILES 字串

COc1cccc(CCN)c1OC

InChI

1S/C10H15NO2/c1-12-9-5-3-4-8(6-7-11)10(9)13-2/h3-5H,6-7,11H2,1-2H3

InChI 密鑰

XKBUFTXNLBWTFP-UHFFFAOYSA-N

一般說明

2,3-Dimethoxyphenethylamine is identified as one of the components in bamboo (Phyllostachys pubescens) plant extract by gas chromatographic- mass spectrometric analysis. 1-(2,3-dimethoxyphenyl)-2-nitroethene undergoes reduction reaction with lithium aluminum hydride (LiAlH4) in the presence of dry tetrahydrofuran to yield 2,3-dimethoxyphenethylamine.

應用

2,3-Dimethoxyphenethylamine may be used in the synthesis of N-(2,3-dimethoxyphenethyl)-2-(3,4-dimethoxyphenyl)acetamide and N-(3,4-dimethoxyphenethyl)-phenyl acetamide.

象形圖

Corrosion
GHS05

訊號詞

Danger

危險聲明

H314

危險分類

Skin Corr. 1B

儲存類別代碼

8B - Non-combustible corrosive hazardous materials

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

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

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Gas chromatography-mass spectrometry analysis and chemical composition of the bamboo-carbonized liquid.
Bilehal D, et al.
Food Analytical Methods, 5(1), 109-112 (2012)
Tetramethoxydibenzoquinolizinium salts. Preparation and antileukemic activity of some positional and structural isomers of coralyne.
Zee-Cheng RKY and Cheng CC.
Journal of Medicinal Chemistry, 19(7), 882-886 (1976)
Chen-Yuan Kuo et al.
European journal of medicinal chemistry, 44(3), 1271-1277 (2008-10-15)
A series of phenoxyisoquinolines, N-phenoxyethyl-1-(2-nitrophenyl)-1,2,3,4-THIQs 3a-3d, N-phenoxyethyl-1-benzyl-1,2,3,4-THIQ 3e, N-phenoxyethyl-1-(2-aminophenyl)-1,2,3,4-THIQs 5f-5i, N-phenoxyethyl-1-(2-phenoxyethylaminophenyl)-1,2,3,4-THIQs 5f'-5i', have been synthesized and tested in isolated rat vas deferens alpha-adrenoreceptors. Comparison of pA2 values for these compounds in the presence of phenylephrine confirms that alpha(1)-adrenoceptor blocking activity

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