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CAS

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360069-41-6

3-iodomethyl-4,5-dimethoxy-benzoic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 360069-41-6 Structure

  • Basic information

    1. Product Name: 3-iodomethyl-4,5-dimethoxy-benzoic acid methyl ester
    2. Synonyms:
    3. CAS NO:360069-41-6
    4. Molecular Formula:
    5. Molecular Weight: 336.126
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 360069-41-6.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: 3-iodomethyl-4,5-dimethoxy-benzoic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-iodomethyl-4,5-dimethoxy-benzoic acid methyl ester(360069-41-6)
    11. EPA Substance Registry System: 3-iodomethyl-4,5-dimethoxy-benzoic acid methyl ester(360069-41-6)

  • 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: 360069-41-6(Hazardous Substances Data)

360069-41-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 360069-41-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,0,0,6 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 360069-41:
(8*3)+(7*6)+(6*0)+(5*0)+(4*6)+(3*9)+(2*4)+(1*1)=126
126 % 10 = 6
So 360069-41-6 is a valid CAS Registry Number.

360069-41-6Relevant articles and documents

Aromatic inhibitors of dehydroquinate synthase: Synthesis, evaluation and implications for gallic acid biosynthesis

Chandran, Sunil S.,Frost

, p. 1493 - 1496 (2007/10/03)

The role of the active site metal in determining binding to 3-dehydroquinate synthase has been examined. Protocatechuic acid, catechol, and derivatives of these aromatics were synthesized that shared the common element of an ortho dihydroxylated benzene ring. Inhibition constants were determined for each aromatic as well as the variation of this inhibition as a function of whether Co+2 or Zn+2 was the active site metal ion.

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