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:
Molecular Weight:
134.13
Beilstein:
1561038
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
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 Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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
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Articles
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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