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Key Documents

541052

Sigma-Aldrich

Ethyl 2,4-dihydroxybenzoate

97%

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About This Item

Linear Formula:
(HO)2C6H3CO2CH2CH3
CAS Number:
Molecular Weight:
182.17
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

assay

97%

mp

69-72 °C (lit.)

SMILES string

CCOC(=O)c1ccc(O)cc1O

InChI

1S/C9H10O4/c1-2-13-9(12)7-4-3-6(10)5-8(7)11/h3-5,10-11H,2H2,1H3

InChI key

BRDIPNLKURUXCU-UHFFFAOYSA-N

Application

Ethyl 2,4-dihydroxybenzoate may be used as a starting reagent to synthesize 4-(ω-bromoalkoxy)benzoates.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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M Lehr et al.
Bioorganic & medicinal chemistry letters, 11(19), 2569-2572 (2001-09-12)
Derivatives of 1-[2-(4-carboxyphenoxy)ethyl]-3-dodecanoylindole-2-carboxylic acid (4) with modified substituents at the indole-1-position were synthesized and evaluated for their ability to inhibit the arachidonic acid release in human platelets mediated by the cytosolic phospholipase A(2). One of the most active compounds obtained

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