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1032401-24-3

C20H29NO2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1032401-24-3 Structure

  • Basic information

    1. Product Name: C20H29NO2
    2. Synonyms:
    3. CAS NO:1032401-24-3
    4. Molecular Formula:
    5. Molecular Weight: 315.456
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1032401-24-3.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: C20H29NO2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C20H29NO2(1032401-24-3)
    11. EPA Substance Registry System: C20H29NO2(1032401-24-3)

  • 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: 1032401-24-3(Hazardous Substances Data)

1032401-24-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1032401-24-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,2,4,0 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1032401-24:
(9*1)+(8*0)+(7*3)+(6*2)+(5*4)+(4*0)+(3*1)+(2*2)+(1*4)=73
73 % 10 = 3
So 1032401-24-3 is a valid CAS Registry Number.

1032401-24-3Upstream product

1032401-24-3Downstream Products

1032401-24-3Relevant articles and documents

Synthesis of dehydro-β-amino esters via highly regioselective amination of allylic carbonates

Benfatti, Fides,Cardillo, Giuliana,Gentilucci, Luca,Mosconi, Elisa,Tolomelli, Alessandra

supporting information; experimental part, p. 2425 - 2428 (2009/05/26)

(Chemical Equation Presented) The allylic amination of acetates and carbonates affords dehydro-β-aminoesters, which are useful precursors of biologically active compounds. The uncatalyzed reaction proceeds via a S N2′ mechanism. On the other hand, under palladium-catalyzed conditions, the reaction shows a strong solvent-dependent regiocontrol, affording exclusively one of the two possible regioisomers with complete transfer of chirality from the substrates to the products.

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