H20008
3-Hydroxybenzoic acid
ReagentPlus®, 99%
Sinónimos:
m-Salicylic acid
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About This Item
Productos recomendados
Quality Level
product line
ReagentPlus®
assay
99%
mp
200-203 °C (lit.)
SMILES string
OC(=O)c1cccc(O)c1
InChI
1S/C7H6O3/c8-6-3-1-2-5(4-6)7(9)10/h1-4,8H,(H,9,10)
InChI key
IJFXRHURBJZNAO-UHFFFAOYSA-N
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Categorías relacionadas
Application
3-Hydroxybenzoic acid, being a component of structural skeleton of various biologically active small molecules, is used in the synthesis of medicinally important compounds such as tyrosine kinase Tie-2 inhibitor, amyloidogenesis inhibitor, antioxidant and anti-inflammatory agents based on oxadiazole analogs of resveratrol.
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Los clientes también vieron
Antioxidant and anti-inflammatory properties of 1, 2, 4-oxadiazole analogs of resveratrol.
Chemico-Biological Interactions, 240, 200-207 (2015)
Evolution of a highly selective and potent 2-(pyridin-2-yl)-1, 3, 5-triazine Tie-2 kinase inhibitor.
Journal of Medicinal Chemistry, 50(4), 611-626 (2007)
Biochemical and structural evaluation of highly selective 2-arylbenzoxazole-based transthyretin amyloidogenesis inhibitors.
Journal of Medicinal Chemistry, 51(2), 260-270 (2007)
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 28(5), 377-384 (2006-06-20)
Solution and solid-state properties of m-hydroxybenzoic acid have been investigated. Two polymorphs were found where the monoclinic modification exhibits a higher stability than the orthorhombic form. The solubility of the monoclinic polymorph was determined between 10 and 50 degrees C
Biochimica et biophysica acta, 1824(3), 433-442 (2011-12-31)
The genome of Rhodococcus jostii RHA1 contains an unusually large number of oxygenase encoding genes. Many of these genes have yet an unknown function, implying that a notable part of the biochemical and catabolic biodiversity of this Gram-positive soil actinomycete
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