3288-52-6 Usage
Uses
Used in Organic Synthesis:
(Z)-2-Cyano-3-hydroxy-but-2-enoic acid methyl ester is used as an intermediate in organic synthesis for the production of various chemical compounds. Its unique structure allows for the creation of a wide range of products, making it a valuable component in this field.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (Z)-2-Cyano-3-hydroxy-but-2-enoic acid methyl ester is used as a key compound in the development of new drugs and pharmaceutical products. Its distinctive properties contribute to the design and synthesis of novel therapeutic agents.
Used in the Production of Fine Chemicals:
(Z)-2-Cyano-3-hydroxy-but-2-enoic acid methyl ester is also utilized in the production of fine chemicals, which are high-purity chemicals used in various applications, including pharmaceuticals, agriculture, and materials science.
Used in the Development of Specialty Materials:
This versatile chemical compound is employed in the development of specialty materials, which are high-performance materials designed for specific applications. Its unique properties make it a valuable component in the creation of these advanced materials.
Check Digit Verification of cas no
The CAS Registry Mumber 3288-52-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,8 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3288-52:
(6*3)+(5*2)+(4*8)+(3*8)+(2*5)+(1*2)=96
96 % 10 = 6
So 3288-52-6 is a valid CAS Registry Number.
3288-52-6Relevant academic research and scientific papers
Anodic cyanation of β-dicarbonyl compounds
Okimoto, Mitsuhiro,Numata, Kaori,Takahashi, Yukio,Hoshi, Masayuki,Tomozawa, Kenta,Shigemoto, Takamasa
, p. 2507 - 2509 (2007/10/03)
Several β-dicarbonyl compounds were electrochemically oxidized in a methanolic solution in the presence of sodium cyanide and sodium methoxide to yield the corresponding α-cyano-β-dicarbonyl compounds in moderate to good yields. Presumably, a two-electron
Aryl halides as precursors of electrogenerated bases. Utilization in coupling reactions of acetonitrile with various electrophilic compounds
Barhdadi, Rachid,Gal, Jacques,Heintz, Monique,Troupel, Michel,Perichon, Jacques
, p. 5091 - 5098 (2007/10/02)
An electrochemical alternative to classical cyanomethylation is possible by using electrogenerated bases (EGBs), obtained by electroreduction of aryl halides in an undivided cell fitted with a cadmium coated cathode and a sacrificial magnesium anode. Acetonitrile is used both as solvent and as hydrogen-active compound. A coupling reaction with various electrophilic compounds was carried out. When the electrophilic compound was present from the beginning of the electrolysis, the expected coupling product with the cyanomethyl anion was obtained. If the electrophilic compound was added only after complete electrolysis of the aryl halide, dimerization of the cyanomethyl anion and a coupling reaction between the dimer anion and the electrophilic compound were observed.
