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Merck
CN

384003

Sigma-Aldrich

2-溴-5-甲氧基苯甲酸

98%

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线性分子式:
BrC6H3(OCH3)CO2H
CAS号:
分子量:
231.04
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

98%

形式

solid

mp

157-159 °C (lit.)

SMILES字符串

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

一般描述

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.

应用

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

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


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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.
Sindelar, K., et al.
Collection of Czechoslovak Chemical Communications, 39(12), 3548-3559 (1974)
Design, synthesis and biological evaluation of the novel isoindolinone derivatives.
Liu J, et al.
J. Chem. Res. (M), 6(9), 256-260 (2014)
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
Amirhossein Fallah et al.
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.
G B BACHMAN et al.
Journal of the American Chemical Society, 68, 1599-1602 (1946-08-01)

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