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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
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Certificates of Analysis (COA)
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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.
Collection of Czechoslovak Chemical Communications, 39(12), 3548-3559 (1974)
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.
J. Chem. Res. (M), 6(9), 256-260 (2014)
Journal of fluorescence, 30(1), 113-120 (2020-01-04)
The detection and sensing of environmentally crucial metal ions has always been of great significance in various fields such as biological and environmental cycles. Our previous studies have indicated a new coumarin based lactone, Urolithin B (i.e., 3-Hydroxy[c]chromen-6-one) as a
Synthesis of substituted aminobenzacridines.
Journal of the American Chemical Society, 68, 1599-1602 (1946-08-01)
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