4-Formylbenzoic acid
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].
Product Specifications
CAS Number
619-66-9
Product Name Alternative
Tetraphthalaldehydic acid
UNSPSC
12352200
Hazard Statement
H302, H315, H319, H335
Target
Biochemical Assay Reagents
Type
Biochemical Assay Reagents
Related Pathways
Others
Field of Research
Others
Assay Protocol
https://www.medchemexpress.com/4-formylbenzoic-acid.html
Purity
99.91
Solubility
DMSO : 100 mg/mL (ultrasonic)
Smiles
C1=C(C=CC(=C1)C=O)C(O)=O
Molecular Formula
C8H6O3
Molecular Weight
150.13
Precautions
H302, H315, H319, H335
References & Citations
[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.
Shipping Conditions
Room Temperature
Storage Conditions
4°C (Powder, stored under nitrogen)
Scientific Category
Biochemical Assay Reagents
Clinical Information
No Development Reported
Available Sizes
Frequently Asked Questions
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