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1393717-21-9

C22H25N3O4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1393717-21-9 Structure

  • Basic information

    1. Product Name: C22H25N3O4
    2. Synonyms: C22H25N3O4
    3. CAS NO:1393717-21-9
    4. Molecular Formula:
    5. Molecular Weight: 395.458
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1393717-21-9.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: C22H25N3O4(CAS DataBase Reference)
    10. NIST Chemistry Reference: C22H25N3O4(1393717-21-9)
    11. EPA Substance Registry System: C22H25N3O4(1393717-21-9)

  • 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: 1393717-21-9(Hazardous Substances Data)

1393717-21-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1393717-21-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,3,7,1 and 7 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1393717-21:
(9*1)+(8*3)+(7*9)+(6*3)+(5*7)+(4*1)+(3*7)+(2*2)+(1*1)=179
179 % 10 = 9
So 1393717-21-9 is a valid CAS Registry Number.

1393717-21-9Downstream Products

1393717-21-9Relevant articles and documents

Intercepted decarboxylative allylations of nitroalkanoates

Schmitt, Meghan,Grenning, Alexander J.,Tunge, Jon A.

, p. 4494 - 4497 (2012)

Using palladium-catalyzed decarboxylation, several cascade reactions of allyl and prenyl nitroalkanoates that lead to nitro-containing chemical building blocks are described. A nitronate Michael addition/Tsuji-Trost allylation cascade was developed, leading to functionally dense chemical building blocks. Likewise, a Tsuji-Trost/decarboxylative protonation sequence was developed for the synthesis of orthogonally functionalized 2° nitroalkanes. The latter method provides rapid access to the indolizidine core.

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