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Merck
모든 사진(1)

문서

533637

Sigma-Aldrich

4-Bromo-2-methoxyphenol

98%

동의어(들):

4-Bromoguaiacol

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모든 사진(1)

About This Item

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

분석

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

픽토그램

Exclamation mark
GHS07

신호어

Warning

유해 및 위험 성명서

H315,H319,H335

Hazard Classifications

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

표적 기관

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves

시험 성적서(COA)

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문서 라이브러리 방문

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
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
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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