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106737-92-2

2-benzoyloxy-4-hydroxybenzaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 106737-92-2 Structure

  • Basic information

    1. Product Name: 2-benzoyloxy-4-hydroxybenzaldehyde
    2. Synonyms: 2-benzoyloxy-4-hydroxybenzaldehyde
    3. CAS NO:106737-92-2
    4. Molecular Formula:
    5. Molecular Weight: 242.231
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 106737-92-2.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: 2-benzoyloxy-4-hydroxybenzaldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-benzoyloxy-4-hydroxybenzaldehyde(106737-92-2)
    11. EPA Substance Registry System: 2-benzoyloxy-4-hydroxybenzaldehyde(106737-92-2)

  • 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: 106737-92-2(Hazardous Substances Data)

106737-92-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106737-92-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,7,3 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 106737-92:
(8*1)+(7*0)+(6*6)+(5*7)+(4*3)+(3*7)+(2*9)+(1*2)=132
132 % 10 = 2
So 106737-92-2 is a valid CAS Registry Number.

106737-92-2Downstream Products

106737-92-2Relevant articles and documents

Conversion of 2,4-dihydroxybenzaldehyde to 2-benzoyloxy-4-hydroxybenzaldehyde and structural characterization of both precursor and product

Hu, Zhiyong,Hardie, Michaele J.,Burckel, Pannee,Pinkerton, A. Alan,Erhardt, Paul W.

, p. 185 - 191 (2007/10/03)

2,4-Dihydroxybenzaldehyde can be acylated at the 2 position if the more reactive 4 position is first protected as the methylmethoxy ether. Deprotection permits isolation of 2-benzoyloxy-4-hydroxybenzaldehyde. 2,4-Dihydroxybenzaldehyde, C7H

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