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Ethanone, 2-mercapto-1-(4-methylphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 23081-11-0 Structure
  • Basic information

    1. Product Name: Ethanone, 2-mercapto-1-(4-methylphenyl)-
    2. Synonyms:
    3. CAS NO:23081-11-0
    4. Molecular Formula: C9H10OS
    5. Molecular Weight: 166.244
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 23081-11-0.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: Ethanone, 2-mercapto-1-(4-methylphenyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ethanone, 2-mercapto-1-(4-methylphenyl)-(23081-11-0)
    11. EPA Substance Registry System: Ethanone, 2-mercapto-1-(4-methylphenyl)-(23081-11-0)
  • 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: 23081-11-0(Hazardous Substances Data)

23081-11-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23081-11-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,8 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 23081-11:
(7*2)+(6*3)+(5*0)+(4*8)+(3*1)+(2*1)+(1*1)=70
70 % 10 = 0
So 23081-11-0 is a valid CAS Registry Number.

23081-11-0Relevant articles and documents

Site-Selective and Enantioselective α,β,γ-Functionalization of 5-Alkylidenefuran-2(5 H)-ones: A Route to Polycyclic γ-Lactones

Skrzyńska, Anna,Frankowski, Sebastian,Moczulski, Marek,Drelich, Piotr,Albrecht, ?ukasz

, p. 1248 - 1252 (2019)

A new strategy for a direct α,β,γ-functionalization of the γ-lactone framework in the corresponding 5-alkylidenefuran-2(5H)-ones is reported. The developed approach is based on a stereocontrolled cascade reaction with 2-mercaptocarbonyl compounds proceedi

Synthesis of Unsymmetrical 1,4-Dicarbonyl Compounds by Photocatalytic Oxidative Radical Additions

Dong, Ya,Li, Ruining,Zhou, Junliang,Sun, Zhankui

supporting information, p. 6387 - 6390 (2021/08/23)

Herein we report a photocatalytic oxidative radical addition reaction for the synthesis of unsymmetrical 1,4-dicarbonyl compounds. This reaction utilizes a desulfurization process to generate electrophilic radicals, which add to α-halogenated alkenes and undergo further oxidation to deliver 1,4-dicarbonyl compounds. This mild and highly efficient method provides a valuable alternative to known strategies.

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