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(S)-(2-methyl-butyl)triphenylphosphonium iodide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 93119-12-1 Structure
  • Basic information

    1. Product Name: (S)-(2-methyl-butyl)triphenylphosphonium iodide
    2. Synonyms: (S)-(2-methyl-butyl)triphenylphosphonium iodide
    3. CAS NO:93119-12-1
    4. Molecular Formula:
    5. Molecular Weight: 460.338
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 93119-12-1.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: (S)-(2-methyl-butyl)triphenylphosphonium iodide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-(2-methyl-butyl)triphenylphosphonium iodide(93119-12-1)
    11. EPA Substance Registry System: (S)-(2-methyl-butyl)triphenylphosphonium iodide(93119-12-1)
  • 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: 93119-12-1(Hazardous Substances Data)

93119-12-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93119-12-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,1,1 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 93119-12:
(7*9)+(6*3)+(5*1)+(4*1)+(3*9)+(2*1)+(1*2)=121
121 % 10 = 1
So 93119-12-1 is a valid CAS Registry Number.

93119-12-1Relevant articles and documents

Total synthesis and configurational validation of (+)-violapyrone C

Lee, Jong Seok,Shin, Junho,Shin, Hee Jae,Lee, Hwa-Sun,Lee, Yeon-Ju,Lee, Hyi-Seung,Won, Hoshik

, p. 4472 - 4476 (2014)

Gold(I)-catalyzed intramolecular 6-endo-dig cyclization of tert-butyl ynoates afforded α-pyrone cores of violapyrones. Moreover, this reaction was successfully applied to the stereospecific syntheses of (+)- and (-)-violapyrone C, which allowed the absolute configuration of natural (+)-violapyrone C to be assigned by comparison of the optical rotations. This first total synthesis, which proceeded in 22% yield over 10 steps from (S)-(-)-2-methylbutanol, features silver(I) oxide promoted monobenzylation of 1,4-butanediol, Wittig olefination, Claisen condensation, Corey-Fuchs reaction, and gold(I)-catalyzed α-pyrone synthesis. Copyright

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