619-66-9
619-66-9
Chemical Structure
4-Formylbenzoic acid
Synonym(s): Tetraphthalaldehydic acid
- CAS No.: 619-66-9
- Formula:C8H6O3
- Molecular Weight:150.13
IUPAC Name: 4-Formylbenzoic acid
InChIKey: GOUHYARYYWKXHS-UHFFFAOYSA-N
SMILES: C1=C(C=CC(=C1)C=O)C(O)=O
Biological Activity: 4-Formylbenzoic acid is an intermediate in the synthesis of terepthalic acid. 4-Formylbenzoic acid can react with barium carbonate to yield two-dimensional barium(II) coordination polymer. 4-Formylbenzoic acid can also be used in the synthesis of acid functionalized mesoporous silica catalyst via the condensation[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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4-Formylbenzoic acid | 99.36% | 4-Formylbenzoic acid is an intermediate in the synthesis of terepthalic acid. 4-Formylbenzoic acid can react with barium carbonate to yield two-dimensional barium(II) coordination polymer. 4-Formylbenzoic acid can also be used in the synthesis of acid functionalized mesoporous silica catalyst via the condensation. | ||||||||||||||||||||
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References
- [1]. M. Haisa, et al., Topochemical studies. VIII. The crystal and molecular sturtures of two polymorphs of 4-formylbenzoic acid. Acta Cryst. (1976). B32, 857-860.
- [2]. Zhao-Peng Deng, et al., 2007. The first two-dimensional barium coordination polymer based on neutral and deprotonated 4-formylbenzoic acid. Applied organometallic chemistry.
- [3]. Sartori, E., et al., (2007). A time-resolved electron paramagnetic resonance investigation of the spin exchange and chemical interactions of reactive free radicals with isotopically symmetric (14N-X-14N) and isotopically asymmetric (14N-X-15N) nitroxyl biradicals. Journal of the American Chemical Society, 129(25), 7785–7792. [Content Brief]
Keywords
