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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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Denis E Markov et al.
The journal of physical chemistry. A, 109(24), 5266-5274 (2006-07-15)
Exciton diffusion and photoluminescence quenching in conjugated polymer/fullerene heterostructures are studied by time-resolved photoluminescence. It is observed that heterostructures consisting of a spin-coated poly(p-phenylene vinylene) (PPV)-based derivative and evaporated C60 are ill-defined because of diffusion of C60 into the polymer
Enzymatic resolution and pharmacological activity of the enantiomers of 3, 5-dihydroxyphenylglycine, a metabotropic glutamate receptor agonist.
Richard BS, et al.
Bioorganic & Medicinal Chemistry Letters, 5(3), 223-228 (1995)
Ivan K Ilic et al.
ChemSusChem, 13(7), 1856-1863 (2020-02-07)
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 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)
A Porel et al.
Indian journal of pharmaceutical sciences, 73(1), 46-56 (2011-12-02)
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
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