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Merck
CN

560197

Sigma-Aldrich

3-溴-4-甲氧基苯乙胺

97%

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About This Item

线性分子式:
BrC6H3(OCH3)(CH2CH2NH2)
分子量:
230.10
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

97%

折射率

n20/D >1.5800 (lit.)

密度

1.389 g/mL at 25 °C (lit.)

官能团

amine
bromo

SMILES字符串

COc1ccc(CCN)cc1Br

InChI

1S/C9H12BrNO/c1-12-9-3-2-7(4-5-11)6-8(9)10/h2-3,6H,4-5,11H2,1H3

InChI key

JHVALSRTUOVNLL-UHFFFAOYSA-N

一般描述

3-Bromo-4-methoxyphenethylamine can be synthesized by reacting N-benzoyl-3-bromo-4-methoxyphenethylamine, acetic acid and HCl in the presence of N2.

应用

3-Bromo-4-methoxyphenethylamine (3-Bromo-4-methoxy-β-phenethylamine) may be used as a starting reagent in the synthesis of 3-bromo-4-methoxy-5-nitro-β-phenethylamine. It may also be used to synthesize 4-bromo-N-(3-bromo-4-methoxyphenethyl)-1H-pyrrole-2-carboxamide.

象形图

Corrosion

警示用语:

Danger

危险声明

危险分类

Eye Dam. 1 - 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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

Total synthesis and biological evaluation of the marine bromopyrrole alkaloid dispyrin: elucidation of discrete molecular targets with therapeutic potential.
Kennedy JP, et al.
Journal of Natural Products, 1783-1786 (2008)
Kumar Saurav et al.
Marine drugs, 18(2) (2020-02-26)
Marine sponges, a well-documented prolific source of natural products, harbor highly diverse microbial communities. Their extracts were previously shown to contain quorum sensing (QS) signal molecules of the N-acyl homoserine lactone (AHL) type, known to orchestrate bacterial gene regulation. Some
Syntheses of the marine metabolites verongamine, hemibastadin-2, and aerothionin using the cyano ylide coupling methodology.
Wasserman HH and Wang J.
The Journal of Organic Chemistry, 63(16), 5581-5586 (1998)
Synthesis of Aminoisoquinolines and Related Compounds. X. A Modified Synthesis of dl-Cularine.
Ishiwata S, et al.
Chemical & Pharmaceutical Bulletin, 18(9), 1850-1855 (1970)

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