126292
3,5-Dimethoxybenzaldehyde
98%
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About This Item
Linear Formula:
(CH3O)2C6H3CHO
CAS Number:
Molecular Weight:
166.17
MDL number:
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
230-772-6
Beilstein/REAXYS Number:
2042374
Assay:
98%
Form:
solid
Quality Level
assay
98%
form
solid
bp
151 °C/16 mmHg (lit.)
mp
45-48 °C (lit.)
functional group
aldehyde
SMILES string
[H]C(=O)c1cc(OC)cc(OC)c1
InChI
1S/C9H10O3/c1-11-8-3-7(6-10)4-9(5-8)12-2/h3-6H,1-2H3
InChI key
VFZRZRDOXPRTSC-UHFFFAOYSA-N
Application
Used frequently as synthetic building block.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
>233.6 °F
flash_point_c
> 112 °C
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Khuzaimah Arifin et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 120, 208-215 (2013-11-05)
A new homoleptic dithiolene tungsten complex, tris-{1,2-bis(3,5-dimethoxyphenyl)-1,2-ethylenodithiolene-S,S'}tungsten, was successfully synthesized via a reaction of the thiophosphate ester and sodium tungstate. The thiophosphate ester was prepared from 3,5-dimethoxybenzaldehyde via benzoin condensation to produce the intermediate 1,2-bis-(3,5-dimethoxyphenyl)-2-hydroxy-ethanone compound, followed by a reaction
Kirsti Parikka et al.
Beilstein journal of organic chemistry, 5, 22-22 (2009-07-11)
The first synthesis of bioactive long alkyl chain 5-n-alkylresorcinols, present in whole grain products, by a novel modification of the Wittig reaction is described. All the main long chain 5-n-alkylresorcinols present in rye and wheat, including C(23) and C(25) analogues
Katie A Keaton et al.
Organic letters, 9(14), 2717-2719 (2007-06-15)
A strategy for ketone synthesis with cyclopropanols as intermediates and its application to (+)-spirolaxine methyl ether is described. The synthesis also features an application of Fu's alkyl-alkyl Suzuki coupling.