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CAS

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349141-24-8

2-(1'-acetoxyethyl)-3,4-dibenzyloxypyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 349141-24-8 Structure

  • Basic information

    1. Product Name: 2-(1'-acetoxyethyl)-3,4-dibenzyloxypyridine
    2. Synonyms:
    3. CAS NO:349141-24-8
    4. Molecular Formula:
    5. Molecular Weight: 377.44
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 349141-24-8.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: 2-(1'-acetoxyethyl)-3,4-dibenzyloxypyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(1'-acetoxyethyl)-3,4-dibenzyloxypyridine(349141-24-8)
    11. EPA Substance Registry System: 2-(1'-acetoxyethyl)-3,4-dibenzyloxypyridine(349141-24-8)

  • 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: 349141-24-8(Hazardous Substances Data)

349141-24-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 349141-24-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,9,1,4 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 349141-24:
(8*3)+(7*4)+(6*9)+(5*1)+(4*4)+(3*1)+(2*2)+(1*4)=138
138 % 10 = 8
So 349141-24-8 is a valid CAS Registry Number.

349141-24-8Relevant articles and documents

Novel synthetic approach to 2-(1′-hydroxyalkyl)- and 2-amido-3-hydroxypyridin-4-ones

Piyamongkol, Sirivipa,Liu, Zu D,Hider, Robert C

, p. 3479 - 3486 (2001)

Novel methods for the synthesis of high pFe3+ iron chelators, 2-(1′-hydroxyalkyl)- and 2-amido-3-hydroxypyridin-4-ones, have been developed. The products are obtained, via N-oxide intermediates, from either maltol or ethyl maltol.

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