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About This Item
Linear Formula:
BrC6H3(OCH3)CO2H
CAS Number:
Molecular Weight:
231.04
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
98%
form
solid
mp
157-159 °C (lit.)
SMILES string
COc1ccc(Br)c(c1)C(O)=O
InChI
1S/C8H7BrO3/c1-12-5-2-3-7(9)6(4-5)8(10)11/h2-4H,1H3,(H,10,11)
InChI key
ODHJOROUCITYNF-UHFFFAOYSA-N
Related Categories
General description
2-Bromo-5-methoxybenzoic acid is a benzoic acid derivative. Synthesis of 2-bromo-5-methoxybenzoic acid and its characterization by HNMR has been reported.
Application
2-Bromo-5-methoxybenzoic acid is suitable for use in the syntheses of urolithin derivatives. It may be used in the synthesis of the following:
- substituted aminobenzacridines
- 8-chloro-2-methoxydibenzo[b,f]thiepin-10(11H)-one and its 3-methoxy derivative
- isoindolinone derivatives
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)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Lynn S Adams et al.
Cancer prevention research (Philadelphia, Pa.), 3(1), 108-113 (2010-01-07)
Estrogen stimulates the proliferation of breast cancer cells and the growth of estrogen-responsive tumors. The aromatase enzyme, which converts androgen to estrogen, plays a key role in breast carcinogenesis. The pomegranate fruit, a rich source of ellagitannins (ET), has attracted
Design, synthesis and biological evaluation of the novel isoindolinone derivatives.
Liu J, et al.
J. Chem. Res. (M), 6(9), 256-260 (2014)
Potential metabolites of clorotepin: 2-and 3-hydroxy derivatives of 8-chloro-10-(4-methylpiperazino)-10, 11-dihydrodibenzo [b, f] thiepin and their methyl ethers.
Sindelar, K., et al.
Collection of Czechoslovak Chemical Communications, 39(12), 3548-3559 (1974)
Synthesis of substituted aminobenzacridines.
G B BACHMAN et al.
Journal of the American Chemical Society, 68, 1599-1602 (1946-08-01)
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