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384003

Sigma-Aldrich

2-溴-5-甲氧基苯甲酸

98%

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About This Item

线性分子式:
BrC6H3(OCH3)CO2H
CAS号:
22921-68-2
分子量:
231.04
EC號碼:
245-329-2
MDL號碼:
MFCD00020214
分類程式碼代碼:
12352100
PubChem物質ID:
24863642
NACRES:
NA.22

品質等級

100

化驗

98%

形狀

solid

mp

157-159 °C (lit.)

官能基

bromo
carboxylic acid

SMILES 字串

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 密鑰

ODHJOROUCITYNF-UHFFFAOYSA-N

相关类别

一般說明

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.

應用

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

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)

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分析证书(COA)

Lot/Batch Number
MKBK4745V
MKBC7564V
MKBC7564
04225HJ
U21097

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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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