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CAS

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1493780-01-0

N,N-dibenzyl-3,3-diisopropoxypropan-1-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1493780-01-0 Structure

  • Basic information

    1. Product Name: N,N-dibenzyl-3,3-diisopropoxypropan-1-amine
    2. Synonyms: N,N-dibenzyl-3,3-diisopropoxypropan-1-amine
    3. CAS NO:1493780-01-0
    4. Molecular Formula:
    5. Molecular Weight: 355.521
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1493780-01-0.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: N,N-dibenzyl-3,3-diisopropoxypropan-1-amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N,N-dibenzyl-3,3-diisopropoxypropan-1-amine(1493780-01-0)
    11. EPA Substance Registry System: N,N-dibenzyl-3,3-diisopropoxypropan-1-amine(1493780-01-0)

  • 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: 1493780-01-0(Hazardous Substances Data)

1493780-01-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1493780-01-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,9,3,7,8 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1493780-01:
(9*1)+(8*4)+(7*9)+(6*3)+(5*7)+(4*8)+(3*0)+(2*0)+(1*1)=190
190 % 10 = 0
So 1493780-01-0 is a valid CAS Registry Number.

1493780-01-0Downstream Products

1493780-01-0Relevant articles and documents

Palladium-catalyzed difunctionalization of enol ethers to amino acetals with aminals and alcohols

Xie, Yinjun,Hu, Jianhua,Xie, Pan,Qian, Bo,Huang, Hanmin

, p. 18327 - 18330 (2013)

A new strategy was developed for intercepting the palladium-alkyl species generated in Heck reaction via nucleophilic addition prior to the step of migratory insertion, which leads to a new palladium-catalyzed difunctionalization of enol ethers with aminals and alcohols to afford amino acetals. Mechanistic studies suggested that the cationic cyclometalated Pd(II) complex generated by the oxidative addition of aminal to a Pd(0) species was crucial for this unusual transformation.

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