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Merck

D109401

Sigma-Aldrich

2,4-Dihydroxybenzoic acid

97%

Sinónimos:

β-Resorcylic acid

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About This Item

Fórmula lineal:
(HO)2C6H3CO2H
Número de CAS:
Peso molecular:
154.12
Beilstein/REAXYS Number:
1946213
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

97%

form

powder

mp

208-211 °C (dec.) (lit.)

SMILES string

OC(=O)c1ccc(O)cc1O

InChI

1S/C7H6O4/c8-4-1-2-5(7(10)11)6(9)3-4/h1-3,8-9H,(H,10,11)

InChI key

UIAFKZKHHVMJGS-UHFFFAOYSA-N

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Application

2,4-Dihydroxybenzoic acid (DHBA) can be used as a starting material for the synthesis of resorcinol-based N-benzyl benzamide derivatives , hydroxylated and prenylated xanthones , and mycophenolic acid.
It can be also used as a reactant in the synthesis of DHBARF polymer aerogels by reacting with formadehyde (F) and resorcinol (R).

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Skin Sens. 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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E W Riddick et al.
Journal of insect science (Online), 19(2) (2019-03-02)
The discovery of inexpensive, readily available bioflavonoids, and their degradation products that boost the reproductive potential of mass-reared predators is the overarching goal of this research. We tested the hypothesis that 2,4-dihydroxybenzoic acid (DHBA), an inexpensive degradation product of morin
The synthesis of mycophenolic acid from 2, 4-dihydroxybenzoic acid
Patterson JW
The Journal of Organic Chemistry, 60(14), 4542-4548 (1995)
Synthesis, SAR and biological evaluation of natural and non-natural hydroxylated and prenylated xanthones as antitumor agents
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The ladybird beetle Stethorus gilvifrons (Mulsant) is an important natural enemy of tetranychid mites and functions as a biological control of these plant pests. The development, survival and reproduction of S. gilvifrons were studied when fed on three artificial diets.

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