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1386262-20-9

C23H24ClNO5S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1386262-20-9 Structure

  • Basic information

    1. Product Name: C23H24ClNO5S
    2. Synonyms: C23H24ClNO5S
    3. CAS NO:1386262-20-9
    4. Molecular Formula:
    5. Molecular Weight: 461.966
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1386262-20-9.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: C23H24ClNO5S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C23H24ClNO5S(1386262-20-9)
    11. EPA Substance Registry System: C23H24ClNO5S(1386262-20-9)

  • 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: 1386262-20-9(Hazardous Substances Data)

1386262-20-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1386262-20-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,6,2,6 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1386262-20:
(9*1)+(8*3)+(7*8)+(6*6)+(5*2)+(4*6)+(3*2)+(2*2)+(1*0)=169
169 % 10 = 9
So 1386262-20-9 is a valid CAS Registry Number.

1386262-20-9Relevant articles and documents

Cu(II)-promoted transformations of α-thienylcarbinols into spirothienooxindoles: Regioselective halogenation of dienyl sulfethers containing electron-rich aryl rings

Yin, Biaolin,Huang, Li,Zhang, Xiaoyu,Ji, Fanghua,Jiang, Huanfeng

, p. 6365 - 6370 (2012/09/22)

Under the promotion of Cu(II) salts, the α-thienylcarbinols with an N-phenyl carbonyl group at the other α-position are converted into three different ranges of spirothienooxindoles involving dearomatizing Friedel-Crafts reaction. In addition, the unprece

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