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533902-34-0

hexanoic acid 1-benzyl-3-(tetrahydrofuran-2-yloxymethoxy)propylamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 533902-34-0 Structure

  • Basic information

    1. Product Name: hexanoic acid 1-benzyl-3-(tetrahydrofuran-2-yloxymethoxy)propylamide
    2. Synonyms: hexanoic acid 1-benzyl-3-(tetrahydrofuran-2-yloxymethoxy)propylamide
    3. CAS NO:533902-34-0
    4. Molecular Formula:
    5. Molecular Weight: 363.497
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 533902-34-0.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: hexanoic acid 1-benzyl-3-(tetrahydrofuran-2-yloxymethoxy)propylamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: hexanoic acid 1-benzyl-3-(tetrahydrofuran-2-yloxymethoxy)propylamide(533902-34-0)
    11. EPA Substance Registry System: hexanoic acid 1-benzyl-3-(tetrahydrofuran-2-yloxymethoxy)propylamide(533902-34-0)

  • 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: 533902-34-0(Hazardous Substances Data)

533902-34-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 533902-34-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,3,9,0 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 533902-34:
(8*5)+(7*3)+(6*3)+(5*9)+(4*0)+(3*2)+(2*3)+(1*4)=140
140 % 10 = 0
So 533902-34-0 is a valid CAS Registry Number.

533902-34-0Downstream Products

533902-34-0Relevant articles and documents

An oxidative entry into the amido trioxadecalin ring system.

Rech, Jason C,Floreancig, Paul E

, p. 1495 - 1498 (2007/10/03)

The amido trioxadecalin ring system is a key structural component of the architecturally interesting anticancer and immunosuppressive agents of the mycalamide, theopederin, and onnamide families of natural products. We report a new entry into this structure in which a mixed acetal serves as a surrogate for a formaldehyde hemiacetal in an addition to an oxidatively generated acyliminium ion. The stereochemical outcome of this process can be explained by the conformational preferences of the product ring system. [reaction: see text]

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