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CAS

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1567950-70-2

C11H20N2O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1567950-70-2 Structure

  • Basic information

    1. Product Name: C11H20N2O2
    2. Synonyms: C11H20N2O2
    3. CAS NO:1567950-70-2
    4. Molecular Formula:
    5. Molecular Weight: 212.292
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1567950-70-2.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: C11H20N2O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C11H20N2O2(1567950-70-2)
    11. EPA Substance Registry System: C11H20N2O2(1567950-70-2)

  • 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: 1567950-70-2(Hazardous Substances Data)

1567950-70-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1567950-70-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,6,7,9,5 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1567950-70:
(9*1)+(8*5)+(7*6)+(6*7)+(5*9)+(4*5)+(3*0)+(2*7)+(1*0)=212
212 % 10 = 2
So 1567950-70-2 is a valid CAS Registry Number.

1567950-70-2Downstream Products

1567950-70-2Relevant articles and documents

A copper-catalyzed coupling reaction of vinyl halides and carbazates: Application in the assembly of polysubstituted pyrroles

Zhou, Chengang,Ma, Dawei

, p. 3085 - 3088 (2014)

CuI-catalyzed coupling of vinyl halides with carbazates gives N-protected N-alkenylhydrazines, which are condensed with ketones under acidic conditions to give polysubstituted pyrroles. The pyrrole synthesis may go through a similar mechanism with Fischer indole synthesis, which involves a [3,3]-sigmatropic rearrangement and other reactions. The Royal Society of Chemistry.

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