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Sigma-Aldrich

Isophthalaldehyde

97%

Synonym(s):

Benzene-1,3-dicarboxaldehyde

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About This Item

Linear Formula:
C6H4-1,3-(CHO)2
CAS Number:
626-19-7
Molecular Weight:
134.13
Beilstein/REAXYS Number:
1561038
EC Number:
210-935-8
MDL number:
MFCD00003372
UNSPSC Code:
12352100
PubChem Substance ID:
24847208
NACRES:
NA.22

assay

97%

mp

87-88 °C (lit.)

SMILES string

O=Cc1cccc(C=O)c1

InChI

1S/C8H6O2/c9-5-7-2-1-3-8(4-7)6-10/h1-6H

InChI key

IZALUMVGBVKPJD-UHFFFAOYSA-N

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General description

Isophthalaldehyde participates in base-catalyzed Knoevenagel condensation reaction.

application

Isophthalaldehyde is used in the synthesis of binuclear ruthenium complex.

Packaging

Packaged in glass bottles

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificates of Analysis (COA)

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The effect of outer-sphere acidity on chemical reactivity in a synthetic heterogeneous base catalyst.
John D Bass et al.
Angewandte Chemie (International ed. in English), 42(42), 5219-5222 (2003-11-06)
Johanna Andersson et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 16(36), 11037-11046 (2010-08-04)
The binuclear ruthenium complex [μ-bidppz(phen)(4)Ru(2)](4+) has been extensively studied since the discovery of its unusual threading intercalation interaction with DNA, a binding mode with extremely slow binding and dissociation kinetics. The complex has been shown to be selective towards long

Articles

Knoevenagel Condensation Reaction

Knoevenagel Condensation is an organic reaction named after Emil Knoevenagel. It is a classic C-C bond formation reaction and a modification of the Aldol Condensation.

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