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533637

4-Bromo-2-methoxyphenol

Name: 4-Bromo-2-methoxyphenol
Brand: ALDRICH

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

NACRES:

NA.22

PubChem Substance ID:

24877979

UNSPSC Code:

12352100

MDL number:

MFCD00051937

Assay:

98%

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Properties

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

Description

pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Novel selective PDE4 inhibitors. 2. Synthesis and structure-activity relationships of 4-aryl-substituted cis-tetra- and cis-hexahydrophthalazinones.

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

A slow, tight binding inhibitor of InhA, the enoyl-acyl carrier protein reductase from Mycobacterium tuberculosis.

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

First asymmetric total syntheses and determination of absolute configurations of (+)-eudesmadiene-12,6-olide and (+)-frullanolide.

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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Global Trade Item Number

SKU	GTIN
533637-25G	04061832287706