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CAS

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1549748-14-2

methyl 4-benzyloxy-2,5-dihydroxybenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1549748-14-2 Structure

  • Basic information

    1. Product Name: methyl 4-benzyloxy-2,5-dihydroxybenzoate
    2. Synonyms: methyl 4-benzyloxy-2,5-dihydroxybenzoate
    3. CAS NO:1549748-14-2
    4. Molecular Formula:
    5. Molecular Weight: 274.273
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1549748-14-2.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: methyl 4-benzyloxy-2,5-dihydroxybenzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 4-benzyloxy-2,5-dihydroxybenzoate(1549748-14-2)
    11. EPA Substance Registry System: methyl 4-benzyloxy-2,5-dihydroxybenzoate(1549748-14-2)

  • 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: 1549748-14-2(Hazardous Substances Data)

1549748-14-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1549748-14-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,4,9,7,4 and 8 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1549748-14:
(9*1)+(8*5)+(7*4)+(6*9)+(5*7)+(4*4)+(3*8)+(2*1)+(1*4)=212
212 % 10 = 2
So 1549748-14-2 is a valid CAS Registry Number.

1549748-14-2Relevant articles and documents

Synthesis of toxyloxanthone B

Giallombardo, Daniele,Nevin, Adam C.,Lewis, William,Nawrat, Christopher C.,Kitson, Russell R.A.,Moody, Christopher J.

, p. 1283 - 1288 (2014)

A synthesis of the naturally occurring xanthone toxyloxanthone B is described, in which the key step is the regioselective addition of a methyl salicylate to a substituted benzyne, followed by cyclization of the intermediate aryl anion to form the xanthon

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