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115665

2-Bromo-4′-methoxyacetophenone

97%

Synonym(s):

ω-Bromo-4-methoxyacetophenone, 4-Methoxyphenacyl bromide

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5 G

$92.00

25 G

$438.00

100 G

$544.50

$92.00


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About This Item

Linear Formula:
CH3OC6H4COCH2Br
CAS Number:
Molecular Weight:
229.07
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
220-118-8
Beilstein/REAXYS Number:
743112
MDL number:
Assay:
97%
Form:
solid

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InChI key

XQJAHBHCLXUGEP-UHFFFAOYSA-N

InChI

1S/C9H9BrO2/c1-12-8-4-2-7(3-5-8)9(11)6-10/h2-5H,6H2,1H3

SMILES string

COc1ccc(cc1)C(=O)CBr

assay

97%

form

solid

mp

69-71 °C (lit.)

functional group

bromo, ketone

storage temp.

2-8°C

Quality Level

Gene Information

human ... PTPN6(5777)

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389390245615115673
assay

97%

assay

97%

assay

95%

assay

98%

Quality Level

100

Quality Level

100

Quality Level

200

Quality Level

100

form

solid

form

solid

form

-

form

-

storage temp.

2-8°C

storage temp.

-

storage temp.

-

storage temp.

2-8°C

mp

69-71 °C (lit.)

mp

47-49 °C (lit.)

mp

94-99 °C (lit.)

mp

60-62 °C (lit.)

functional group

bromo

functional group

bromo, fluoro, ketone

functional group

bromo, ketone, nitro

functional group

bromo, ketone

Application

2-Bromo-4′-methoxyacetophenone has been used in the synthesis of light-responsive diblock copolymers containing para-methoxyphenacyl photocleavable side groups.

pictograms

CorrosionExclamation mark

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

target_organs

Respiratory system

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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Synthesis of diblock copolymers bearing p-methoxyphenacyl side groups.
Polym. Chem., 2(10), 2284-2292 (2011)
Guido J Noguera et al.
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 78, 190-197 (2015-07-27)
A set of 4-arylthiazolylhydrazones derived from 1-indanones (TZHs) previously synthesized and assayed against Trypanosoma cruzi, the causative agent of Chagas disease, were explored in terms of conformational analysis. We found that TZHs can adopt four minimum energy conformations: cis (A
Daniel I Perez et al.
Journal of medicinal chemistry, 54(12), 4042-4056 (2011-04-20)
Development of kinase-targeted therapies for central nervous system (CNS) diseases is a great challenge. Glycogen synthase kinase 3 (GSK-3) offers a great potential for severe CNS unmet diseases, being one of the inhibitors on clinical trials for different tauopathies. Following

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