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Assay
97%
mp
127-130 °C (lit.)
functional group
ester
SMILES string
CCOC(=O)c1cc(O)cc(O)c1
InChI
1S/C9H10O4/c1-2-13-9(12)6-3-7(10)5-8(11)4-6/h3-5,10-11H,2H2,1H3
InChI key
APHYVLPIZUVDTK-UHFFFAOYSA-N
General description
Ethyl 3,5-dihydroxybenzoate is a dihydroxybenzoic ester. It can be synthesized from 3,5-dihydroxybenzoic acid by esterification process with absolute ethanol.
Application
Ethyl 3,5-dihydroxybenzoate may be used as a starting reagent in the synthesis of ethyl 3,5-bis(ω-hydroxyoligo(ethyleneoxy))benzoates and p-alkoxycarbonylated palladium bis(phosphinite) PCP pincer complexes.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - 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
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PCP-Bis (phosphinite) pincer complexes: new homogeneous catalysts for a-arylation of ketones.
Tetrahedron Letters, 47(19), 3233-3237 (2006)
Structural variants of hyperbranched polyesters.
Macromolecules, 29(7), 2524-2530 (1996)
Journal of agricultural and food chemistry, 57(14), 6224-6230 (2009-07-16)
Tannase is an enzyme with important biotechnological applications in the food industry. Previous studies have identified the tannase encoding gene in Lactobacillus plantarum and also have reported the description of the purification of recombinant L. plantarum tannase through a protocol
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