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1116669-83-0

C20H17NO3S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1116669-83-0 Structure

  • Basic information

    1. Product Name: C20H17NO3S
    2. Synonyms: C20H17NO3S
    3. CAS NO:1116669-83-0
    4. Molecular Formula:
    5. Molecular Weight: 351.426
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1116669-83-0.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: C20H17NO3S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C20H17NO3S(1116669-83-0)
    11. EPA Substance Registry System: C20H17NO3S(1116669-83-0)

  • 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: 1116669-83-0(Hazardous Substances Data)

1116669-83-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1116669-83-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,1,6,6,6 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1116669-83:
(9*1)+(8*1)+(7*1)+(6*6)+(5*6)+(4*6)+(3*9)+(2*8)+(1*3)=160
160 % 10 = 0
So 1116669-83-0 is a valid CAS Registry Number.

1116669-83-0Downstream Products

1116669-83-0Relevant articles and documents

A Palladium-Catalyzed Oxa-(4+4)-Cycloaddition Strategy towards Oxazocine Scaffolds

Scuiller, Ana?s,Liu, Xueyang,Cordier, Marie,Garrec, Julian,Archambeau, Alexis

, p. 981 - 986 (2021)

A Pd-catalyzed oxa-(4+4)-cycloaddition between 1-azadienes and (2-hydroxymethyl)allyl carbonates is described. Aurone-derived azadienes furnished polycyclic 1,5-oxazocines in good yields. Interestingly, linear azadienes have also been involved and yielded monocyclic heterocycles with complete regioselectivity. DFT calculations were carried out to gain insight on this observation.

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