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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-935-8
Beilstein/REAXYS Number:
1561038
MDL number:
Assay:
97%
Quality Level
assay
97%
mp
87-88 °C (lit.)
functional group
aldehyde
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
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
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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.
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)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 115282-5G | 04061838703200 |
| 115282-25G | 04061838703194 |