Skip to Content
Merck
All Photos(2)

Key Documents

252743

Sigma-Aldrich

1-Bromo-2,5-dimethoxybenzene

98%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
BrC6H3(OCH3)2
CAS Number:
Molecular Weight:
217.06
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

refractive index

n20/D 1.57 (lit.)

bp

130-131 °C/10 mmHg (lit.)

density

1.445 g/mL at 25 °C (lit.)

functional group

bromo

SMILES string

COc1ccc(OC)c(Br)c1

InChI

1S/C8H9BrO2/c1-10-6-3-4-8(11-2)7(9)5-6/h3-5H,1-2H3

InChI key

DWCGNRKFLRLWCJ-UHFFFAOYSA-N

Application

1-Bromo-2,5-dimethoxybenzene has been used in preparation of:
  • S-(-)-2-[N-(trifluoroacetyl)amino]-1-(2,5-dimethoxy-4- bromophenyl)-1-propanone
  • 1,4-bis{4-[2-(4-pyridyl)ethenyl]phenyl}butadiyne and 1,4-bis{2,5-dimethoxy-4-[2-(4-pyridyl)ethenyl]phenyl}butadiyne
  • 1-bromo-4-iodo-2,5-dimethoxybenzene

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Synthesis and photophysical properties of new two-photon absorption chromophores containing a diacetylene moiety as the central p-bridge.
Iwase Y, et al.
Journal of Materials Chemistry, 13(7), 1575-1581 (2003)
Shape-persistent V-shaped mesogens-formation of nematic phases with biaxial order.
Lehmann M, et al.
Journal of Materials Chemistry, 16(44), 4326-4334 (2006)
Richard A Glennon et al.
Journal of medicinal chemistry, 47(24), 6034-6041 (2004-11-13)
Activation of 5-HT(2A) serotonin receptors represents a novel approach to lowering intraocular pressure. Because 5-HT(2A) serotonin receptor agonists might also produce undesirable central effects should sufficient quantities enter the brain, attempts were made to identify 5-HT(2) serotonin receptor agonists with

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service