T2207
Terephthalaldehyde
ReagentPlus®, 99%
Synonym(s):
Benzene-1,4-dicarboxaldehyde, Terephthaldicarboxaldehyde
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About This Item
Linear Formula:
C6H4(CHO)2
CAS Number:
Molecular Weight:
134.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-784-8
Beilstein/REAXYS Number:
385863
MDL number:
Assay:
99%
product line
ReagentPlus®
assay
99%
bp
245-248 °C (lit.)
mp
114-116 °C (lit.)
SMILES string
[H]C(=O)c1ccc(cc1)C([H])=O
InChI
1S/C8H6O2/c9-5-7-1-2-8(6-10)4-3-7/h1-6H
InChI key
KUCOHFSKRZZVRO-UHFFFAOYSA-N
Application
Terephthalaldehyde can be used as a starting material for:
- The synthesis of fused bis-benzoquinoline derivatives on reacting with arylamines and cyclic ketones through one pot three component reaction.
- The photochemical synthesis of 5,10-disubstituted[5]helicenes by reacting with benzyl cyanide via Knoevenagel reaction.
- The synthesis of a nitronyl nitroxide (NIT) radical with a pyrimidiniumolate unit, which are useful precursors for building molecular magnets.
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 1
ppe
Eyeshields, Gloves, type N95 (US)
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Synthesis of dipolar nitronyl nitroxides
Greve S, et al.
Organic Letters, 2(15), 2269-2270 (2000)
Camphorsulfonic acid catalyzed one-pot three-component reaction for the synthesis of fused quinoline and benzoquinoline derivatives
Gattu R, et al.
The Journal of Organic Chemistry, 82(23), 12416-12429 (2017)
Facile photochemical synthesis of 5, 10-disubstituted [5] Helicenes by removing molecular orbital degeneracy
Ito N, et al.
Organic Letters, 16(9), 2502-2505 (2014)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| T2207-100G | 04061837341717 |
| T2207-500G | 04061837341724 |
| T2207-5G | 04061837341786 |