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Salicylic Acid Methyl Ether-d3 is an isotopically labeled derivative of salicylic acid, a compound commonly utilized in organic synthesis. This deuterated form is characterized by the presence of deuterium atoms, which can provide unique properties and applications in various chemical and biological processes.

96739-36-5

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96739-36-5 Usage

Uses

Used in Organic Synthesis:
Salicylic Acid Methyl Ether-d3 is used as a synthetic building block for the preparation of various organic compounds. Its incorporation of deuterium atoms can offer distinct advantages in terms of reaction kinetics, selectivity, and stability, making it a valuable tool in the development of new chemical entities.
Used in Pharmaceutical Research:
In the pharmaceutical industry, Salicylic Acid Methyl Ether-d3 can be employed as a labeled reference compound for the study of drug metabolism and pharmacokinetics. The presence of deuterium can help in tracing the metabolic pathways and understanding the behavior of the compound in biological systems.
Used in Analytical Chemistry:
Salicylic Acid Methyl Ether-d3 can be utilized as an internal standard in analytical techniques such as mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy. The deuterium-labeled compound can improve the accuracy and precision of quantitative measurements by providing a stable reference point.
Used in Material Science:
In the field of material science, Salicylic Acid Methyl Ether-d3 can be used to study the properties of polymers and other materials. The incorporation of deuterium can provide insights into the structure, dynamics, and interactions of these materials at the molecular level.
Overall, Salicylic Acid Methyl Ether-d3 is a versatile compound with applications spanning across various industries, including organic synthesis, pharmaceutical research, analytical chemistry, and material science. Its unique properties, particularly the presence of deuterium atoms, make it a valuable tool for advancing scientific understanding and developing innovative solutions.

Check Digit Verification of cas no

The CAS Registry Mumber 96739-36-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,7,3 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 96739-36:
(7*9)+(6*6)+(5*7)+(4*3)+(3*9)+(2*3)+(1*6)=185
185 % 10 = 5
So 96739-36-5 is a valid CAS Registry Number.

96739-36-5Downstream Products

96739-36-5Relevant academic research and scientific papers

Cycloreversal reaction and ortho interactions in 2-Aryl-4H-3,1-benzoxazin-4-ones on electron

Ramana,Kantharaj

, p. 1195 - 1200 (1995)

A cycloreversal reaction, leading to aroyl cations, is the major process in 2-aryl-4H-3,1-benzoxazin-4-ones under electron impact conditions. The ortho interaction of the methoxy and the nitro groups in the 2-phenyl moieties in these compounds present the most abundant ions at m/z 119 and 134, respectively, in their mass spectra as a result of the transfer of a hydrogen atom from the former and an oxygen atom from the latter to the imine nitrogen of the heterocycle. The ion structures and the mechanisms for the proposed fragmentations are based on high-resolution data, B/E and B2/E linked-scan spectra, collision-activated decomposition-B-/E linked-scan spectra and deuterium labelling.

Rearrangements and Isomerism in the Molecular Ion of o-Methoxybenzoic Acid

Gillis, Richard G.,Porter, Quentin N.

, p. 82 - 84 (2007/10/02)

The molecular ion of o-methoxy-d3-benzoic acid can unddergo three different rearrangements and hydrogen/deruterium exchange between the functional groups.This can result in 14 isomers of the molecular ion before it decomposes giving fragments a

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