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Merck
CN

441074

2-溴-4,5-二甲氧基苯甲酸

98%

别名:

6-溴藜芦酸

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关于此项目

线性分子式:
BrC6H2(OCH3)2CO2H
化学文摘社编号:
分子量:
261.07
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
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产品名称

2-溴-4,5-二甲氧基苯甲酸, 98%

InChI

1S/C9H9BrO4/c1-13-7-3-5(9(11)12)6(10)4-8(7)14-2/h3-4H,1-2H3,(H,11,12)

SMILES string

COc1cc(Br)c(cc1OC)C(O)=O

InChI key

HWFCHCRFQWEFMU-UHFFFAOYSA-N

assay

98%

mp

188-190 °C (lit.)

functional group

bromo
carboxylic acid

Quality Level

Application

2-Bromo-4,5-dimethoxybenzoic acid may be used as starting material for the synthesis of norathyriol and urolithins.

General description

2-Bromo-4,5-dimethoxybenzoic acid is a 2-halo-4,5-dialkoxybenzoic acid derivative.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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历史批次信息供参考:

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Hideyuki Ito et al.
Journal of agricultural and food chemistry, 56(2), 393-400 (2008-01-01)
Hydrolyzable tannins, including ellagitannins, occur in foods such as berries and nuts. Various biological activities, including antioxidant, antiviral, and antitumor activities, have been noted and reported for ellagitannins, but the absorption and metabolism of purified ellagitannins are poorly understood. We
A facile synthesis of norathyriol.
Qin Q-X, et al.
J. Chem. Res. (M), 37(1), 38-39 (2013)
Peter Lorenz et al.
Chemistry & biodiversity, 15(5), e1800035-e1800035 (2018-03-27)
Seeds from Hypericum species have recently been identified as an interesting source of xanthone derivatives. Extraction of seeds from H. perforatum with MeOH and subsequent concentration via polyamide adsorption yielded a fraction enriched in tetrahydroxyxanthones (THX), which were further semipurified
Sashi G Kasimsetty et al.
Journal of agricultural and food chemistry, 57(22), 10636-10644 (2009-11-19)
The cytochrome P450 enzyme, CYP1B1, is an established target in prostate cancer chemoprevention. Compounds inhibiting CYP1B1 activity are contemplated to exert beneficial effects at three stages of prostate cancer development, that is, initiation, progression, and development of drug resistance. Pomegranate

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