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Merck
CN

115282

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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24847208
EC Number:
210-935-8
Beilstein/REAXYS Number:
1561038
MDL number:
MFCD00003372

Key Documents

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Product Name

Isophthalaldehyde, 97%

InChI key

IZALUMVGBVKPJD-UHFFFAOYSA-N

InChI

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

SMILES string

O=Cc1cccc(C=O)c1

assay

97%

mp

87-88 °C (lit.)

functional group

aldehyde

Quality Level

200

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Application

Isophthalaldehyde is used in the synthesis of binuclear ruthenium complex.

General description

Isophthalaldehyde participates in base-catalyzed Knoevenagel condensation reaction.

Packaging

Packaged in glass bottles

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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Certificates of Analysis (COA)

Lot/Batch Number
BCCN2964
BCCM0013
BCCK2263
BCCG9328
BCCD4935

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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
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)

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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