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C21H26N2O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 500699-23-0 Structure
  • Basic information

    1. Product Name: C21H26N2O2
    2. Synonyms:
    3. CAS NO:500699-23-0
    4. Molecular Formula:
    5. Molecular Weight: 338.45
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 500699-23-0.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: C21H26N2O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C21H26N2O2(500699-23-0)
    11. EPA Substance Registry System: C21H26N2O2(500699-23-0)
  • 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: 500699-23-0(Hazardous Substances Data)

500699-23-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 500699-23-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,0,6,9 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 500699-23:
(8*5)+(7*0)+(6*0)+(5*6)+(4*9)+(3*9)+(2*2)+(1*3)=140
140 % 10 = 0
So 500699-23-0 is a valid CAS Registry Number.

500699-23-0Upstream product

500699-23-0Downstream Products

500699-23-0Relevant articles and documents

Hydride-donor abilities of 1,4-dihydropyridines: A comparison with π nucleophiles and borohydride anions

Richter, Dorothea,Mayr, Herbert

, p. 1958 - 1961 (2009)

(Chemical Equation Presented) How are dihydropyridines like indoles? Both groups of compounds have similar nucleophilicity parameters N and are therefore suitable substrates for iminium-catalyzed reactions of α,β- unsaturated aldehydes. The N parameters of 1,4-dihydropyridines were derived from the rates of hydride transfer reactions to benzhydrylium ions (see scheme).

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