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4-Fluorobenzoyl chloride-[carbonyl-13C]

General Information
Catalog: BLP-010951
CAS: 91742-47-1
Molecular Formula: C6[13C]H4ClFO
Molecular Weight: 159.55
Chemical Structure
4-Fluorobenzoyl chloride-[carbonyl-13C]
Synonyms 4-Fluorobenzoyl-(carbonyl-13C) chloride
Related CAS 403-43-0 (unlabelled)
Canonical SMILES C1=CC(=CC=C1C(=O)Cl)F
InChI InChI=1S/C7H4ClFO/c8-7(10)5-1-3-6(9)4-2-5/h1-4H/i7+1
InChI Key CZKLEJHVLCMVQR-CDYZYAPPSA-N
Purity 99% atom 13C
Density 1.35 g/cm3 at 25°C (lit.)

4-Fluorobenzoyl chloride-[carbonyl-13C] is a chemical compound utilized as a labeled reagent in cutting-edge scientific investigations. Here are key applications of 4-Fluorobenzoyl chloride-[carbonyl-13C] presented with high perplexity and burstiness:

Isotope Labeling in Analytical Chemistry: Widely employed in isotope labeling for NMR and mass spectrometry endeavors, 4-Fluorobenzoyl chloride-[carbonyl-13C] plays a pivotal role. The integration of the [carbonyl-13C] isotope permits precise monitoring of molecular dynamics and interactions within intricate mixtures. This facilitates in-depth insights into structural intricacies and mechanistic details essential for deciphering chemical phenomena.

Drug Metabolism Studies: In the domain of pharmacokinetics, 4-Fluorobenzoyl chloride-[carbonyl-13C] assumes a crucial role in tracing drug metabolism and distribution pathways. Through carbon-13 labeling of drug entities, researchers can track the destiny of pharmaceutical compounds within the body. This methodology aids in pinpointing metabolites, understanding metabolic routes, and optimizing drug formulations for heightened therapeutic efficiency.

Synthesis of Labeled Compounds: Serving as a pivotal intermediate in crafting carbon-13 labeled aromatic substances, 4-Fluorobenzoyl chloride-[carbonyl-13C] holds significant importance. These labeled compounds are indispensable for research across diverse sectors like material sciences and bioorganic chemistry. The ability to introduce specific isotopes facilitates investigations into molecular interactions and reaction dynamics, enriching scientific explorations.

Environmental Research: Acting as a tracer in environmental inquiries, the compound sheds light on the destiny and displacement of pollutants in the ecosystem. The distinctive isotopic fingerprint of 4-Fluorobenzoyl chloride-[carbonyl-13C] empowers researchers to trace chemical metamorphoses and degradation processes in environmental samples. This data plays a pivotal role in evaluating the impact of pollutants and formulating effective mitigation strategies.

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