52110-55-1 Usage
Uses
Used in Pharmaceutical Industry:
MUCIDIN is used as an antifungal agent for treating fungal infections. It targets and inhibits the respiratory chain in fungi, thereby disrupting their energy production and growth. This makes MUCIDIN a crucial component in the development of antifungal medications and treatments.
Used in Agricultural Industry:
MUCIDIN is used as a fungicide for protecting crops from various fungal diseases. Its broad-spectrum antifungal activity allows it to be effective against a wide range of fungal pathogens, helping to maintain crop health and yield. By incorporating MUCIDIN into agricultural practices, farmers can reduce the reliance on chemical fungicides and promote more sustainable farming methods.
Used in Research and Development:
MUCIDIN is used as a research tool for studying fungal biology and pathogenesis. Its unique mode of action and potent antifungal properties make it an invaluable compound for investigating the mechanisms of fungal infections and the development of resistance. Additionally, MUCIDIN can be used to identify new targets for antifungal drug development and to understand the complex interactions between fungi and their hosts.
Check Digit Verification of cas no
The CAS Registry Mumber 52110-55-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,1,1 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 52110-55:
(7*5)+(6*2)+(5*1)+(4*1)+(3*0)+(2*5)+(1*5)=71
71 % 10 = 1
So 52110-55-1 is a valid CAS Registry Number.
InChI:InChI=1/C16H18O3/c1-13(15(12-18-2)16(17)19-3)8-7-11-14-9-5-4-6-10-14/h4-12H,1-3H3/b11-7+,13-8-,15-12+
52110-55-1Relevant articles and documents
Dehydration-type Ti-Claisen Condensation (Carbonhomologation) of α-Heteroatom-substituted Acetates with Alkyl Formates: Utilization as (Z)-Stereodefined Cross-coupling Partners and Application to Concise Synthesis of Strobilurin A
Nakatsuji, Hidefumi,Kamada, Risa,Kitaguchi, Hideya,Tanabe, Yoo
, p. 3865 - 3879 (2017/11/15)
TiCl4?Et3N or ?Bu3N reagent conducted a highly (Z)-stereoselective carbon homologation (dehydration type Ti-Claisen condensation) of alkyl α-heteroatom (halo and sulfonyloxy)-substituted acetates (XCH2CO2R) with alkyl formates (HCO2R) to afford various alkyl β-alkoxy-α-halo or sulfonyloxy-substituted acrylates (24 examples; 51%–91% yield). Stereoretentive Suzuki-Miyaura, Negishi, and Sonogashira cross-couplings using the obtained methyl β-methoxy-α-halo or sulfonyloxy-substituted acrylates proceeded smoothly to produce a variety of β-alkoxy-α-substituted acrylates in moderate to high yield (35 examples; 29%–99% yield). As a successful application, a 3-step straightforward synthesis of strobilurin A was performed utilizing the present reaction sequence (dehydration type Ti-Claisen condensation and Suzuki-Miyaura cross-coupling), wherein the geometry of the three consecutive olefins (2E,3Z,5E) was completely maintained. (Figure presented.).
STEREOCONTROLLED SYNTHESES OF STROBILURIN A AND ITS (9E)-ISOMER
Beautement, Kevin,Clough, John M.
, p. 475 - 478 (2007/10/02)
The (E,Z,E)-configuration (1) of the strobilurins has been confirmed by stereocontrolled synthesis.
