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368113

Sigma-Aldrich

3,5-Dihydroxybenzaldehyde

98%

Sinônimo(s):

α-Resorcylaldehyde (6CI)

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About This Item

Fórmula linear:
(HO)2C6H3CHO
Número CAS:
26153-38-8
Peso molecular:
138.12
Beilstein:
1930147
Número CE:
247-479-4
Número MDL:
MFCD00016611
Código UNSPSC:
12352100
ID de substância PubChem:
24862890
NACRES:
NA.22

Ensaio

98%

pf

153-158 °C (lit.)

cadeia de caracteres SMILES

[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

chave InChI

HAQLHRYUDBKTJG-UHFFFAOYSA-N

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Descrição geral

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

Aplicação

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)

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

Certificados de análise (COA)

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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
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)
Synthesis and photochromism of E, E-3, 4-(3, 5-dimethoxybenzylidene) succinic anhydride and its infra red active 2-dicyanomethylene derivative.
Asiri AM.
Journal of Photochemistry and Photobiology A: Chemistry, 159(1), 1-5 (2003)
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