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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

Curated Selection

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