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4-Fluorobenzyl Alcohol-[2,3,5,6-d4]

General Information
Catalog: BLP-010563
CAS: 93111-26-3
Molecular Formula: C7H3D4FO
Molecular Weight: 130.15
Chemical Structure
4-Fluorobenzyl Alcohol-[2,3,5,6-d4]
Synonyms 4-Fluorobenzyl-2,3,5,6-d4 Alcohol; p-Fluorobenzyl Alcohol-d4; (4-Fluorophenyl)methanol-d4; 4-Fluorobenzenemethanol-d4; NSC 63347-d4; p-Fluorophenylmethanol-d4; (4-fluorophenyl-2,3,5,6-d4)methanol; Benzene-2,3,5,6-d4-methanol, 4-fluoro-
IUPAC Name (2,3,5,6-tetradeuterio-4-fluorophenyl)methanol
Related CAS 459-56-3 (unlabelled)
Canonical SMILES C1=CC(=CC=C1CO)F
InChI InChI=1S/C7H7FO/c8-7-3-1-6(5-9)2-4-7/h1-4,9H,5H2/i1D,2D,3D,4D
InChI Key GEZMEIHVFSWOCA-RHQRLBAQSA-N
Purity 98% atom D
Solubility Slightly soluble in Water
Appearance Colorless Liquid
Storage Store at RT

4-Fluorobenzyl Alcohol-[2,3,5,6-d4], a deuterated compound with distinctive isotopic labeling, finds diverse applications across various scientific fields. Here are key applications presented with high perplexity and burstiness:

Pharmaceutical Research: This essential deuterated compound plays a pivotal role in advancing drug metabolism studies, shedding light on the intricate pharmacokinetics of novel pharmaceuticals. By closely monitoring the deuterium label, researchers unravel the mysteries of drug metabolism and clearance processes within the body, offering crucial insights for optimizing drug design and enhancing therapeutic efficacy.

NMR Spectroscopy: Widely recognized in the realm of nuclear magnetic resonance (NMR) spectroscopy, 4-Fluorobenzyl Alcohol-[2,3,5,6-d4] stands out as a reference standard with its deuterium atoms that aid in untangling complex molecular structures. The distinct isotopic labeling minimizes signal overlap in intricate mixtures, facilitating detailed analyses of molecular architectures. This application proves invaluable in deciphering the complexities of organic compounds.

Chemical Synthesis: A cornerstone in organic chemistry, this labeled compound serves as a potent tool for tracing reaction pathways and mechanisms, revolutionizing mechanistic studies and synthetic route optimizations. By introducing deuterated atoms into starting materials, chemists meticulously track the journey of specific atoms during chemical transformations, unlocking fundamental insights into the intricacies of chemical reactions.

Environmental Studies: Equipped with a unique isotopic signature, 4-Fluorobenzyl Alcohol-[2,3,5,6-d4] emerges as a pivotal tracer in environmental research, instrumental in examining pollutant dispersion and degradation within ecosystems. Researchers harness its distinct isotopic label to investigate the environmental destiny of chemical substances, enabling a comprehensive understanding of ecological impacts and environmental sustainability.

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