Stable isotope labeling allows researchers to study metabolic pathways in vivo in a safe manner.
Stable isotope-labeled compounds are used as environmental pollutant standards for the detection of air, water, soil, sediment and food.
In addition to treating various diseases, isotopes are used for imaging, diagnosis, and newborn screening.
Small molecule compounds labeled with stable isotopes can be used as chemical reference for chemical identification, qualitative, quantitative, detection, etc. Various types of NMR solvents can be used to study the structure, reaction mechanism and reaction kinetics of compounds.
Stable isotope labeling allows researchers to study metabolic pathways in vivo in a safe manner.
Stable isotope-labeled compounds are used as environmental pollutant standards for the detection of air, water, soil, sediment and food.
General Information |
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Catalog: BLP-005758 |
Molecular Formula: C7H5DO2 |
Molecular Weight: 123.13 |
Chemical Structure |
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Description | 4-Hydroxybenzaldehyde-2-[d] is an isotope analogue of 4-Hydroxybenzaldehyde (p-Hydroxybenzaldehyde). p-Hydroxybenzaldehyde is one of the major components in Dendrocalamus asper bamboo shoots, with antagonistic effect on GABAA receptor of the α1β2γ2S subtype at high concentrations. |
IUPAC Name | (4E)-3-deuterio-4-(hydroxymethylidene)cyclohexa-2,5-dien-1-one |
Related CAS | 123-08-0 (unlabelled) |
Canonical SMILES | C1=CC(=CC=C1C=O)O |
InChI | InChI=1S/C7H6O2/c8-5-6-1-3-7(9)4-2-6/h1-5,8H/i1D/b6-5- |
InChI Key | RGHHSNMVTDWUBI-MICDWDOJSA-N |
Melting Point | 117-119°C |
Purity | 99% by CP; 97% atom D |
Appearance | White Solid |
4-Hydroxybenzaldehyde-2-[d] stands as a significant compound in research and industrial realms, showcasing versatility and utility across diverse fields. Here are key applications of 4-Hydroxybenzaldehyde-2-[d] presented with high perplexity and burstiness:
Chemical Synthesis: Acting as a fundamental building block in synthetic chemistry, 4-Hydroxybenzaldehyde-2-[d] plays a crucial role in crafting complex organic molecules. Its utility extends to serving as a precursor for the synthesis of pharmaceuticals, agrochemicals, and dyes, fostering the emergence of novel compounds. With its adaptable chemical properties allowing for diverse modifications, this compound emerges as a versatile intermediate in organic syntheses, driving innovation in chemical manufacturing.
Pharmaceutical Research: Positioned at the forefront of drug discovery and development, 4-Hydroxybenzaldehyde-2-[d] finds application in the pharmaceutical industry. Its structural characteristics make it conducive to forming components of bioactive compounds under scrutiny for therapeutic potentials. Researchers leverage its properties to engender derivatives, unlocking various pharmacological activities and refining drug efficacy and selectivity, propelling advancements in medical science.
Perfume and Flavor Industry: Swaying the perfume and flavor landscape, 4-Hydroxybenzaldehyde-2-[d] emerges as a vital ingredient in fragrance and flavor formulation. Bestowed with aromatic allure, it elevates products with a captivating scent, becoming a sought-after choice for perfumes and scented goods. Moreover, its usage extends to enriching flavor profiles of diverse food and beverage items, introducing a sweet almond-like essence, enhancing sensorial experiences.
Biochemical Research: Unveiling its utility in biochemical assays, 4-Hydroxybenzaldehyde-2-[d] assumes roles as a substrate or reagent in enzyme-driven reactions. Particularly in its deuterated form, it proves instrumental in isotopic labeling studies, enabling researchers to trace and analyze metabolic pathways diligently. This aids in unraveling enzyme mechanisms and scrutinizing reaction kinetics within intricate biological systems, fostering deeper insights into biochemical processes.
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