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Sigma-Aldrich

3,5-Dimethoxybenzaldehyde

98%

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About This Item

Linear Formula:
(CH3O)2C6H3CHO
CAS Number:
Molecular Weight:
166.17
Beilstein:
2042374
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

>233.6 °F

Flash Point(C)

> 112 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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.
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

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