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Sigma-Aldrich

3-Bromo-4-methoxyphenethylamine

97%

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About This Item

Linear Formula:
BrC6H3(OCH3)(CH2CH2NH2)
CAS Number:
159465-27-7
Molecular Weight:
230.10
MDL number:
MFCD00153891
UNSPSC Code:
12352100
PubChem Substance ID:
24879852
NACRES:
NA.22

assay

97%

refractive index

n20/D >1.5800 (lit.)

density

1.389 g/mL at 25 °C (lit.)

SMILES string

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

General description

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

application

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.

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Synthesis of Aminoisoquinolines and Related Compounds. X. A Modified Synthesis of dl-Cularine.
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Total synthesis and biological evaluation of the marine bromopyrrole alkaloid dispyrin: elucidation of discrete molecular targets with therapeutic potential.
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Journal of Natural Products, 1783-1786 (2008)
Syntheses of the marine metabolites verongamine, hemibastadin-2, and aerothionin using the cyano ylide coupling methodology.
Wasserman HH and Wang J.
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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

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