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432792

Sigma-Aldrich

Methyl 2,6-dihydroxybenzoate

97%

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About This Item

Linear Formula:
(HO)2C6H3CO2CH3
CAS Number:
Molecular Weight:
168.15
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

97%

form

solid

mp

67-70 °C (lit.)

functional group

ester

SMILES string

COC(=O)c1c(O)cccc1O

InChI

1S/C8H8O4/c1-12-8(11)7-5(9)3-2-4-6(7)10/h2-4,9-10H,1H3

InChI key

WCQZCKUNZVMBDC-UHFFFAOYSA-N

General description

Methyl 2,6-dihydroxybenzoate can be synthesized from 2,6-dihydroxybenzoic acid.[1] Multiple fluorescences in methyl 2,6-dihydroxybenzoate have been investigated. Its short wavelength (387) and long wavelength (500) emissions are reported to arise from extramolecularly hydrogen-bonded and intramolecularly hydrogen-bonded species.[2]

Application

Methyl 2,6-dihydroxybenzoate may be used for the preparation of methyl 2-hydroxy-6-methoxybenzoate[1] and oxamyl propionic acid.[3]

pictograms

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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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Hydroxy-methoxybenzoic methyl esters: synthesis and antifeedant activity on the pine weevil, Hylobius abietis.
Legrand S, et al.
Zeitschrift fur Naturforschung, B: Chemical Sciences, 59(7), 829-835 (2004)
U Mennen
South African journal of surgery. Suid-Afrikaanse tydskrif vir chirurgie, 30(4), 184-186 (1992-12-01)
A new method to restore flexion of fingers is described whereby the plantaris tendon (or part of the tendo Achillis), with its bony insertion, is transferred to the finger. Strong bony anchorage is achieved in the distal phalanx, while a
Multiple fluorescences iii. methyl 2, 6-dihydroxybenzoate and methyl salicylate.
Kosower EM and Dodiuk H.
Journal of Luminescence, 11(3), 249-254 (1976)

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