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1100268-43-6

C22H20N2O8S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1100268-43-6 Structure

  • Basic information

    1. Product Name: C22H20N2O8S
    2. Synonyms: C22H20N2O8S
    3. CAS NO:1100268-43-6
    4. Molecular Formula:
    5. Molecular Weight: 472.475
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1100268-43-6.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: C22H20N2O8S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C22H20N2O8S(1100268-43-6)
    11. EPA Substance Registry System: C22H20N2O8S(1100268-43-6)

  • 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: 1100268-43-6(Hazardous Substances Data)

1100268-43-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1100268-43-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,0,2,6 and 8 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1100268-43:
(9*1)+(8*1)+(7*0)+(6*0)+(5*2)+(4*6)+(3*8)+(2*4)+(1*3)=86
86 % 10 = 6
So 1100268-43-6 is a valid CAS Registry Number.

1100268-43-6Downstream Products

1100268-43-6Relevant articles and documents

Stereoselective synthesis of trisubstituted alkenes containing (Z)-allylthio units from the acetates of Baylis-Hillman adducts

Liu, Yunkui,Xu, Danqian,Xu, Zhenyuan,Zhang, Yongmin

, p. 188 - 198 (2008/09/18)

A series of trisubstituted alkenes containing (Z)-allylthio moieties as key structural units, that is, sodium (Z)-allyl thiosulfates, symmetrical di(Z-allyl) sulfides, and di(Z-allyl) disulfides, unsymmetrical diallyl sulfides were prepared in moderate to

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