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126292

Sigma-Aldrich

3,5-Dimethoxybenzaldehyde

98%

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About This Item

Fórmula lineal:
(CH3O)2C6H3CHO
Número de CAS:
7311-34-4
Peso molecular:
166.17
Beilstein/REAXYS Number:
2042374
EC Number:
230-772-6
MDL number:
MFCD00003366
UNSPSC Code:
12352100
PubChem Substance ID:
24847713
NACRES:
NA.22

assay

98%

form

solid

bp

151 °C/16 mmHg (lit.)

mp

45-48 °C (lit.)

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

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Application

Used frequently as synthetic building block.

Storage Class

11 - Combustible Solids

wgk_germany

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
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.
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
Marco Bandini et al.
Organic letters, 9(11), 2151-2153 (2007-05-08)
A new poly(ethylene glycol)-modified DAT2-Cu(OAc)2 complex smoothly catalyzes a base-free nitroaldol condensation in a highly enantioselective manner (ee up to 93%) also in reagent-grade solvent and in the presence of air. Effective recovery and recycling (up to five runs) of
Johannes Taeger et al.
Oncology letters, 16(1), 654-659 (2018-06-22)
Despite partial advances in therapy for patients suffering from head and neck squamous cell carcinomas (HNSCC), prognosis still remains poor with minimal improvement in survival for over the last several decades. Some agents found are known to cause cancer cell
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