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110043-77-1

22-O-Tosyl-12-epi-pleuromutilin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 110043-77-1 Structure

  • Basic information

    1. Product Name: 22-O-Tosyl-12-epi-pleuromutilin
    2. Synonyms:
    3. CAS NO:110043-77-1
    4. Molecular Formula:
    5. Molecular Weight: 532.698
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 110043-77-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 22-O-Tosyl-12-epi-pleuromutilin(CAS DataBase Reference)
    10. NIST Chemistry Reference: 22-O-Tosyl-12-epi-pleuromutilin(110043-77-1)
    11. EPA Substance Registry System: 22-O-Tosyl-12-epi-pleuromutilin(110043-77-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 110043-77-1(Hazardous Substances Data)

110043-77-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 110043-77-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,0,4 and 3 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 110043-77:
(8*1)+(7*1)+(6*0)+(5*0)+(4*4)+(3*3)+(2*7)+(1*7)=61
61 % 10 = 1
So 110043-77-1 is a valid CAS Registry Number.

110043-77-1Relevant articles and documents

Synthesis and in vitro antibacterial activity of four novel pleuromutilin derivatives

Tang, Youzhi,Luo, Jian,Chen, Xiaojie,Wang, Bo,Shen, Xiangguang,Liu, Jianhua

, p. 1537 - 1540 (2013)

Four novel pleuromutilin derivatives with butyl amine group in the C-14 side-chain were designed, synthesized and confirmed by FT-IR, 1H-NMR and HRMS. The results of antibacterial activity showed that the antibacterial activity of pleuromutilin derivative

Inversion of Configuration of the Vinylgroup at Carbon 12 by Reversible Retro-En-Cleavage

Berner, Heinz,Vyplel, Hermann,Schulz, Gerhard,Schneider, Helmut

, p. 1073 - 1080 (2007/10/02)

The reaction of pleuromutilin-22-O-tosylat(2) with EtZnI afforded a mixture of the 12-epimeric compounds 2 and 3.A reversible retro-en-reaction of the homoallylic system is discussed as a possible mechanistic pathway.The structure assignment is based on 1H- and 13C-NMR spectroscopic data. - Keywords: Pleuromutilin; Inversion of configuration; Reversible retro-en-cleavage; Simmons-Smith-reaction; Type I-"metallo-en"-reaction

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