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533637

Sigma-Aldrich

4-Bromo-2-methoxyphenol

98%

Synonym(s):

4-Bromoguaiacol

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About This Item

Linear Formula:
BrC6H3(OCH3)OH
CAS Number:
7368-78-7
Molecular Weight:
203.03
MDL number:
MFCD00051937
UNSPSC Code:
12352100
PubChem Substance ID:
24877979
NACRES:
NA.22

assay

98%

mp

34-37 °C (lit.)

SMILES string

COc1cc(Br)ccc1O

InChI

1S/C7H7BrO2/c1-10-7-4-5(8)2-3-6(7)9/h2-4,9H,1H3

InChI key

WHSIIJQOEGXWSN-UHFFFAOYSA-N

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCBS3442V
BCBH1850V
BCBD4598V
BCBB1690V
BCBB1690

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M Van der Mey et al.
Journal of medicinal chemistry, 44(16), 2523-2535 (2001-07-27)
A series of 4-aryl-substituted cis-4a,5,8,8a-tetra- and cis-4a,5,6,7,8,8a-hexahydro-2H-phthalazin-1-ones with high inhibitory activity toward cAMP-specific phosphodiesterase (PDE4) was synthesized. To study structure-activity relationships various substituents were introduced to the 2-, 3-, and 4-positions of the 4-phenyl ring. Substitution at the 4-position of
Sylvia R Luckner et al.
The Journal of biological chemistry, 285(19), 14330-14337 (2010-03-05)
InhA, the enoyl-ACP reductase in Mycobacterium tuberculosis is an attractive target for the development of novel drugs against tuberculosis, a disease that kills more than two million people each year. InhA is the target of the current first line drug
Florian Juhlke et al.
Frontiers in chemistry, 5, 120-120 (2018-01-13)
Chlorinated guaiacol derivatives are found in waste water of pulp mills using chlorine in the bleaching process of wood pulp. They can also be detected in fish tissue, possibly causing off-odors. To date, there is no systematic investigation on the
Yu-Yu Chou et al.
Organic letters, 15(7), 1584-1587 (2013-03-15)
The first asymmetric total syntheses of sesquiterpene lactones (+)-eudesmadiene-12,6-olide (1) and (+)-frullanolide (2) have been accomplished from 4-bromo-2-methoxyphenol (5) in 12 and 13 synthetic steps, respectively, and the absolute configurations of these two natural products were determined.

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