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101220-62-6

(difluoromethyl)(mesityl)selane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 101220-62-6 Structure

  • Basic information

    1. Product Name: (difluoromethyl)(mesityl)selane
    2. Synonyms: (difluoromethyl)(mesityl)selane
    3. CAS NO:101220-62-6
    4. Molecular Formula:
    5. Molecular Weight: 249.162
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 101220-62-6.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: (difluoromethyl)(mesityl)selane(CAS DataBase Reference)
    10. NIST Chemistry Reference: (difluoromethyl)(mesityl)selane(101220-62-6)
    11. EPA Substance Registry System: (difluoromethyl)(mesityl)selane(101220-62-6)

  • 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: 101220-62-6(Hazardous Substances Data)

101220-62-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101220-62-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,2,2 and 0 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 101220-62:
(8*1)+(7*0)+(6*1)+(5*2)+(4*2)+(3*0)+(2*6)+(1*2)=46
46 % 10 = 6
So 101220-62-6 is a valid CAS Registry Number.

101220-62-6Downstream Products

101220-62-6Relevant articles and documents

Metal-Free Difluoromethylselenolation of Arylamines under Visible-Light Photocatalysis

Lu, Kui,Li, Quan,Xi, Xiaolan,Zhou, Ting,Zhao, Xia

, p. 1224 - 1231 (2020)

A novel visible-light photocatalytic difluoromethylselenolation of aryl amines via in situ generation of aryldiazonium salts was achieved using Se-(difluoromethyl) 4-methylbenzenesulfonoselenoate, which was synthesized for the first time. The reagent is readily accessible and shelf-stable. The metal-free reaction conditions and the broad substrate scope provide a green protocol for the efficient and rapid introduction of the difluoromethylselenylether group.

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