441074
2-Bromo-4,5-dimethoxybenzoic acid
98%
Synonym(s):
6-Bromoveratric acid
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About This Item
Linear Formula:
BrC6H2(OCH3)2CO2H
CAS Number:
Molecular Weight:
261.07
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
98%
mp
188-190 °C (lit.)
SMILES string
COc1cc(Br)c(cc1OC)C(O)=O
InChI
1S/C9H9BrO4/c1-13-7-3-5(9(11)12)6(10)4-8(7)14-2/h3-4H,1-2H3,(H,11,12)
InChI key
HWFCHCRFQWEFMU-UHFFFAOYSA-N
Related Categories
General description
2-Bromo-4,5-dimethoxybenzoic acid is a 2-halo-4,5-dialkoxybenzoic acid derivative.
Application
2-Bromo-4,5-dimethoxybenzoic acid may be used as starting material for the synthesis of norathyriol and urolithins.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Hideyuki Ito et al.
Journal of agricultural and food chemistry, 56(2), 393-400 (2008-01-01)
Hydrolyzable tannins, including ellagitannins, occur in foods such as berries and nuts. Various biological activities, including antioxidant, antiviral, and antitumor activities, have been noted and reported for ellagitannins, but the absorption and metabolism of purified ellagitannins are poorly understood. We
Peter Lorenz et al.
Chemistry & biodiversity, 15(5), e1800035-e1800035 (2018-03-27)
Seeds from Hypericum species have recently been identified as an interesting source of xanthone derivatives. Extraction of seeds from H. perforatum with MeOH and subsequent concentration via polyamide adsorption yielded a fraction enriched in tetrahydroxyxanthones (THX), which were further semipurified
A facile synthesis of norathyriol.
Qin Q-X, et al.
J. Chem. Res. (M), 37(1), 38-39 (2013)
Sashi G Kasimsetty et al.
Journal of agricultural and food chemistry, 57(22), 10636-10644 (2009-11-19)
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