368113
3,5-Dihydroxybenzaldehyde
98%
Synonym(s):
α-Resorcylaldehyde (6CI)
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About This Item
Linear Formula:
(HO)2C6H3CHO
CAS Number:
Molecular Weight:
138.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
247-479-4
Beilstein/REAXYS Number:
1930147
MDL number:
Assay:
98%
Product Name
3,5-Dihydroxybenzaldehyde, 98%
InChI key
HAQLHRYUDBKTJG-UHFFFAOYSA-N
InChI
1S/C7H6O3/c8-4-5-1-6(9)3-7(10)2-5/h1-4,9-10H
SMILES string
[H]C(=O)c1cc(O)cc(O)c1
assay
98%
mp
153-158 °C (lit.)
functional group
aldehyde
Quality Level
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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)
General description
Condensation of isopropyl ethers of p-hydroxyphenyl acetic acid and 3,5-dihydroxybenzaldehyde has been reported.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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 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
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)
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
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