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CAS

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72709-44-5

N-Methyl-5-(4-methylphenoxy)phthalamic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 72709-44-5 Structure

  • Basic information

    1. Product Name: N-Methyl-5-(4-methylphenoxy)phthalamic acid
    2. Synonyms:
    3. CAS NO:72709-44-5
    4. Molecular Formula:
    5. Molecular Weight: 285.299
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 72709-44-5.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: N-Methyl-5-(4-methylphenoxy)phthalamic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-Methyl-5-(4-methylphenoxy)phthalamic acid(72709-44-5)
    11. EPA Substance Registry System: N-Methyl-5-(4-methylphenoxy)phthalamic acid(72709-44-5)

  • 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: 72709-44-5(Hazardous Substances Data)

72709-44-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72709-44-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,7,0 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 72709-44:
(7*7)+(6*2)+(5*7)+(4*0)+(3*9)+(2*4)+(1*4)=135
135 % 10 = 5
So 72709-44-5 is a valid CAS Registry Number.

72709-44-5Downstream Products

72709-44-5Relevant articles and documents

Diaryl Ether Formation via Nitro Displacement with 4-Methylphenol and Potassium Carbonate on 4-Nitro-N-methylphthalimide

Relles, Howard M.,Johnson, Donald S.,Dellacoletta, B. A.

, p. 1374 - 1379 (2007/10/02)

Conditions for the equilibration between a nitro-substituted imide and its ring-opened amide-acid salt were established.Evidence was found that nitro displacement by an aryl oxide nucleophile occured only in the imide form.Extensive 13C NMR data are presented as structural evidence and for distinguishing amide acid isomers.

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