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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.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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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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