D109606
2,6-Dihydroxybenzoic acid
98%
Synonym(s):
γ-Resorcylic acid
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Assay
98%
form
powder
mp
165 °C (dec.) (lit.)
SMILES string
OC(=O)c1c(O)cccc1O
InChI
1S/C7H6O4/c8-4-2-1-3-5(9)6(4)7(10)11/h1-3,8-9H,(H,10,11)
InChI key
AKEUNCKRJATALU-UHFFFAOYSA-N
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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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Organic letters, 11(4), 871-874 (2009-01-28)
The facile preparation of a novel 8-membered polyhydroxylated salicylic acid lactone from 2,6-dihydroxybenzoic acid and sodium thio-D-glucose is described. The key step involved a sodium hydride promoted intramolecular lactonization in the presence of excess TMSCl, which led to isolation of
Environmental technology, 33(13-15), 1517-1522 (2012-09-20)
The paper mainly focused on illustrating the merit of respirometric analysis in assessing the inhibitory/toxic impact of xenobiotics on substrate biodegradation. It also evaluated biodegradation characteristics of these chemicals at continuous exposure through acclimation ofthe microbial culture. The nature and
Archives of microbiology, 181(6), 391-397 (2004-05-01)
A nonoxidative decarboxylase, 2,6-dihydroxybenzoate decarboxylase, was found in Agrobacterium tumefaciens IAM12048. The enzyme activity was induced specifically by 2,6-dihydroxybenzoate. The purified enzyme was a homotetramer of identical 38 kDa subunits. The purified decarboxylase catalyzed the nonoxidative decarboxylation of 2,6-dihydroxybenzoate and
Journal of bacteriology, 189(5), 1573-1581 (2006-12-13)
We identified a gene cluster that is involved in the gamma-resorcylate (2,6-dihydroxybenzoate) catabolism of the aerobic bacterium Rhizobium sp. strain MTP-10005. The cluster consists of the graRDAFCBEK genes, and graA, graB, graC, and graD were heterologously expressed in Escherichia coli.
Angewandte Chemie (International ed. in English), 48(7), 1283-1286 (2009-01-14)
An extremophilic challenge: Stereospecific condensation of a fully functionalized ketal aldehyde and a 2,6-dihydroxybenzoic acid is the key step in the synthesis of (-)-berkelic acid confirming Fürstner's reassignment of the stereochemistry at C18 and C19, establishing the absolute stereochemistry, and
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