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368113

Sigma-Aldrich

3,5-Dihydroxybenzaldehyde

98%

Sinónimos:

α-Resorcylaldehyde (6CI)

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About This Item

Fórmula lineal:
(HO)2C6H3CHO
Número de CAS:
26153-38-8
Peso molecular:
138.12
Beilstein/REAXYS Number:
1930147
EC Number:
247-479-4
MDL number:
MFCD00016611
UNSPSC Code:
12352100
PubChem Substance ID:
24862890
NACRES:
NA.22

assay

98%

mp

153-158 °C (lit.)

SMILES string

[H]C(=O)c1cc(O)cc(O)c1

InChI

1S/C7H6O3/c8-4-5-1-6(9)3-7(10)2-5/h1-4,9-10H

InChI key

HAQLHRYUDBKTJG-UHFFFAOYSA-N

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General description

Condensation of isopropyl ethers of p-hydroxyphenyl acetic acid and 3,5-dihydroxybenzaldehyde has been reported.

Application

3,5-Dihydroxybenzaldehyde is suitable for use in the synthesis of 3,5-dihydroxyphenylglycine (3,5-DHPG). It may be used in the synthesis of:
  • fulgide7
  • 3,5-bis(undeca-4,6-diynyloxy)benzaldehyde
  • 3,5-didodecyloxybenzaldehyde
  • 1′-methyl-1′,5′-dihydro-2′-(3,5-bis(undeca-4,6-diynyloxy)phenyl)-1H-pyrrolo[3′,4′:1,9](C60-Ih)[5,6]fullerene (F2D)

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Asiri AM.
Journal of Photochemistry and Photobiology A: Chemistry, 159(1), 1-5 (2003)
A re-investigation of resveratrol synthesis by Perkins reaction. Application to the synthesis of aryl cinnamic acids.
Solladie G, et al.
Tetrahedron, 59(18), 3315-3321 (2003)
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Although several recent publications describe cathodes for electrochemical energy storage materials made from regrown biomass in aqueous electrolytes, their transfer to lithium-organic batteries is challenging. To gain a deeper understanding, we investigate the influences on charge storage in model systems
A Porel et al.
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The aim of the present study was the development and subsequent validation of a simple, precise and stability-indicating reversed phase HPLC method for the simultaneous determination of guaifenesin, terbutaline sulphate and bromhexine hydrochloride in the presence of their potential impurities
Xuewu Sui et al.
The Journal of biological chemistry, 290(51), 30212-30223 (2015-10-27)
Carotenoid cleavage oxygenases (CCOs) are non-heme, Fe(II)-dependent enzymes that participate in biologically important metabolic pathways involving carotenoids and apocarotenoids, including retinoids, stilbenes, and related compounds. CCOs typically catalyze the cleavage of non-aromatic double bonds by dioxygen (O2) to form aldehyde
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