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1414891-09-0

C20H31N3Se is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1414891-09-0 Structure

  • Basic information

    1. Product Name: C20H31N3Se
    2. Synonyms: C20H31N3Se
    3. CAS NO:1414891-09-0
    4. Molecular Formula:
    5. Molecular Weight: 392.446
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1414891-09-0.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: C20H31N3Se(CAS DataBase Reference)
    10. NIST Chemistry Reference: C20H31N3Se(1414891-09-0)
    11. EPA Substance Registry System: C20H31N3Se(1414891-09-0)

  • 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: 1414891-09-0(Hazardous Substances Data)

1414891-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1414891-09-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,4,8,9 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1414891-09:
(9*1)+(8*4)+(7*1)+(6*4)+(5*8)+(4*9)+(3*1)+(2*0)+(1*9)=160
160 % 10 = 0
So 1414891-09-0 is a valid CAS Registry Number.

1414891-09-0Downstream Products

1414891-09-0Relevant articles and documents

4-Organochalcogenoyl-1H-1,2,3-triazoles: Synthesis and functionalization by a nickel-catalyzed Negishi cross-coupling reaction

Stefani, Helio A.,Leal, Daiana M.,Manarin, Flavia

, p. 6495 - 6499,5 (2012)

A general method for the synthesis of triazoles containing selenium and tellurium was accomplished via a CuCAAC reaction between organic azides and a terminal triple bond, generated by in situ deprotection of the silyl group. The reaction tolerates alkyl and arylazides, with alkyl and aryl substituents directly bonded to the chalcogen atom. The products were readily functionalized by a nickel-catalyzed Negishi cross-coupling reaction, furnishing the aryl-heteroaryl products at the 4-position in good yields.

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