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1379799-58-2

C22H24N2O2S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1379799-58-2 Structure

  • Basic information

    1. Product Name: C22H24N2O2S
    2. Synonyms: C22H24N2O2S
    3. CAS NO:1379799-58-2
    4. Molecular Formula:
    5. Molecular Weight: 380.511
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1379799-58-2.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: C22H24N2O2S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C22H24N2O2S(1379799-58-2)
    11. EPA Substance Registry System: C22H24N2O2S(1379799-58-2)

  • 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: 1379799-58-2(Hazardous Substances Data)

1379799-58-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1379799-58-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,9,7,9 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1379799-58:
(9*1)+(8*3)+(7*7)+(6*9)+(5*7)+(4*9)+(3*9)+(2*5)+(1*8)=252
252 % 10 = 2
So 1379799-58-2 is a valid CAS Registry Number.

1379799-58-2Relevant articles and documents

Sequential ring-closing metathesis-vinyl halide Heck cyclization reactions: Access to the tetracyclic ring system of ervitsine

Bennasar, M.-Llu?sa,Zulaica, Ester,Solé, Daniel,Alonso, Sandra

, p. 4641 - 4648 (2012)

A chemoselective indole-templated ring-closing metathesis is used to assemble the cyclohepta[b]indole substructure of the indole alkaloid ervitsine. A subsequent intramolecular Heck coupling of the resulting alkene functionality with an amino-tethered vinyl halide accomplishes the closure of the unique 2-azabicyclo[4.3.1]decane framework of the alkaloid with concomitant incorporation of the exocyclic E-ethylidene substituent.

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