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108009-48-9

4,6-dichloroisophthalaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 108009-48-9 Structure

  • Basic information

    1. Product Name: 4,6-dichloroisophthalaldehyde
    2. Synonyms: 4,6-dichloroisophthalaldehyde
    3. CAS NO:108009-48-9
    4. Molecular Formula:
    5. Molecular Weight: 203.025
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 108009-48-9.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: 4,6-dichloroisophthalaldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4,6-dichloroisophthalaldehyde(108009-48-9)
    11. EPA Substance Registry System: 4,6-dichloroisophthalaldehyde(108009-48-9)

  • 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: 108009-48-9(Hazardous Substances Data)

108009-48-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108009-48-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,0,0 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 108009-48:
(8*1)+(7*0)+(6*8)+(5*0)+(4*0)+(3*9)+(2*4)+(1*8)=99
99 % 10 = 9
So 108009-48-9 is a valid CAS Registry Number.

108009-48-9Downstream Products

108009-48-9Relevant articles and documents

Reactions of 2-Cyclohexen-1-ones and Cyclohexane-1,3-diones with Chloro Methylene Iminium Salts

Katritzky, Alan R.,Marson, Charles M.

, p. 2726 - 2730 (2007/10/02)

Products are isolated and pathways established for the reactions of cyclohexane-1,3-diones with Vilsmeier reagents.Similarities between those reactions and the reactions of some 2-cyclohexen-1-ones with Vilsmeier reagents are demonstrated.The pathways proposed allow rationalization of products formed by the action of Vilsmeier reagents on a variety of cyclic and acyclic ketones.

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