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1428318-78-8

C20H21N3O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1428318-78-8 Structure

  • Basic information

    1. Product Name: C20H21N3O2
    2. Synonyms: C20H21N3O2
    3. CAS NO:1428318-78-8
    4. Molecular Formula:
    5. Molecular Weight: 335.406
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1428318-78-8.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: C20H21N3O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C20H21N3O2(1428318-78-8)
    11. EPA Substance Registry System: C20H21N3O2(1428318-78-8)

  • 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: 1428318-78-8(Hazardous Substances Data)

1428318-78-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1428318-78-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,8,3,1 and 8 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1428318-78:
(9*1)+(8*4)+(7*2)+(6*8)+(5*3)+(4*1)+(3*8)+(2*7)+(1*8)=168
168 % 10 = 8
So 1428318-78-8 is a valid CAS Registry Number.

1428318-78-8Downstream Products

1428318-78-8Relevant articles and documents

Halogen exchange (Halex) reaction of 5-iodo-1,2,3-triazoles: Synthesis and applications of 5-fluorotriazoles

Worrell, Brady T.,Hein, Jason E.,Fokin, Valery V.

, p. 11791 - 11794 (2013/01/15)

A good exchange: 5-Iodo-1,2,3-triazoles undergo facile substitution reactions with fluoride salts, thus providing ready access to 5-fluorotriazoles (see scheme). The latter can be further elaborated with various nucleophiles to furnish fully substituted 1,2,3-triazole compounds. Copyright

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