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55063-97-3

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55063-97-3 Usage

Description

METHYL METHACRYLATE-3,3-D2, with the CAS number 55063-97-3, is an isotopically labeled research compound that is utilized in various scientific studies and experiments. It is a deuterated version of methyl methacrylate, which means it contains deuterium atoms instead of regular hydrogen atoms. This characteristic makes it valuable for research purposes, particularly in the field of chemistry and materials science.

Uses

Used in Research and Development:
METHYL METHACRYLATE-3,3-D2 is used as a research compound for conducting experiments and investigations in the field of chemistry and materials science. The presence of deuterium atoms in the compound allows researchers to study its properties and behavior under different conditions, which can lead to a better understanding of the compound's structure and potential applications.
Used in Polymer Synthesis:
METHYL METHACRYLATE-3,3-D2 is used as a monomer in the synthesis of isotopically labeled polymers. These polymers can be employed in various applications, such as in the development of new materials with specific properties or in the study of polymerization processes.
Used in Analytical Chemistry:
METHYL METHACRYLATE-3,3-D2 is used as a reference material in analytical chemistry. The deuterated compound can be utilized to calibrate instruments and improve the accuracy of measurements, particularly in techniques that involve mass spectrometry or nuclear magnetic resonance (NMR) spectroscopy.
Used in Pharmaceutical Research:
METHYL METHACRYLATE-3,3-D2 can be used as a starting material or intermediate in the synthesis of isotopically labeled pharmaceutical compounds. These labeled compounds can be valuable for studying drug metabolism, pharmacokinetics, and drug-protein interactions, ultimately contributing to the development of more effective and safer medications.
Used in Environmental Studies:
METHYL METHACRYLATE-3,3-D2 can be employed in environmental research to study the fate and transport of pollutants in the environment. The deuterated compound can be used as a tracer to track the movement and distribution of contaminants, providing valuable insights into their behavior and potential impact on ecosystems.

Check Digit Verification of cas no

The CAS Registry Mumber 55063-97-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,0,6 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 55063-97:
(7*5)+(6*5)+(5*0)+(4*6)+(3*3)+(2*9)+(1*7)=123
123 % 10 = 3
So 55063-97-3 is a valid CAS Registry Number.

55063-97-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name METHYL METHACRYLATE-3,3-D2

1.2 Other means of identification

Product number -
Other names 3,3-dideuterio-2-methyl-acrylic acid methyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:55063-97-3 SDS

55063-97-3Downstream Products

55063-97-3Relevant articles and documents

Palladium(II)-Catalyzed Asymmetric Acetalization of Alkenes

Hosokawa, Takahiro,Yamanaka, Toshio,Itotani, Motohiro,Murahashi, Shun-Ichi

, p. 6159 - 6167 (2007/10/03)

The terminal olefinic carbon of N-methaacryloyl-2-oxazolidinones is smoothly acetalized by alcohols in the presence of PdCl2 catalyst.The use of 4(S)-isopropyl-, phenyl-, and tert-butyl-2-oxazolidinones as the chiral auxiliary resulted in the formation of the corresponding (2'S)-acetals in 61, 80, and 95percent de, respectively.Reductive removal of the auxiliary with LiAlH4 followed by deacetalization produced (R)-3-hydroxy-2-methylpropanal.The enantiomer of this compound, derived from 4(R)-substituted oxazolidinones, served as a building block for synthesizing a 1β-methylcarbapenem precursor in high enantiomeric excess.In the acetalization of 3',3'-dideuteriated methacryloyl-4-isopropyloxazolidinone with MeOH, one D-atom on the terminal olefinic carbon stereoselectively migrated to the chiral center in the product acetal.On the basis of this 1,2-hydride migration and the conformational preference of the methacryloyl moiety, the reaction pathway and the mechanism of the diastereoselection are discussed.

The synthesis of deuterated methyl methacrylates

Ayrey,Wong

, p. 935 - 944,939,940,943 (2007/10/06)

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