Skip to Content
Merck
All Photos(1)

Key Documents

More Documents

115282

Sigma-Aldrich

Isophthalaldehyde

97%

Synonym(s):

Benzene-1,3-dicarboxaldehyde

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
C6H4-1,3-(CHO)2
CAS Number:
626-19-7
Molecular Weight:
134.13
Beilstein:
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

Looking for similar products? Visit Product Comparison Guide

Related Categories

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

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service