384003
2-溴-5-甲氧基苯甲酸
98%
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关于此项目
线性分子式:
BrC6H3(OCH3)CO2H
化学文摘社编号:
分子量:
231.04
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
245-329-2
MDL number:
Assay:
98%
Form:
solid
Quality Segment
assay
98%
form
solid
mp
157-159 °C (lit.)
functional group
bromo, carboxylic acid
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
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
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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)
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)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 384003-5G | 04061831965261 |