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Merck
CN

115665

2-Bromo-4′-methoxyacetophenone

97%

Synonym(s):

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

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About This Item

Linear Formula:
CH3OC6H4COCH2Br
CAS Number:
2632-13-5
Molecular Weight:
229.07
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24847233
EC Number:
220-118-8
Beilstein/REAXYS Number:
743112
MDL number:
MFCD00000201

Key Documents

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Product Name

2-Bromo-4′-methoxyacetophenone, 97%

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

100

Gene Information

human ... PTPN6(5777)

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Related Categories

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
GHS05,GHS07

signalword

Danger

hcodes

H314,H335

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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Certificates of Analysis (COA)

Lot/Batch Number
BCCK6468
BCCK3823
BCCG7229
BCCG2307
STBJ7685

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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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