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81118-43-6

3-decylthio-N-methyl-5-nitrophthalimide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 81118-43-6 Structure

  • Basic information

    1. Product Name: 3-decylthio-N-methyl-5-nitrophthalimide
    2. Synonyms: 3-decylthio-N-methyl-5-nitrophthalimide
    3. CAS NO:81118-43-6
    4. Molecular Formula:
    5. Molecular Weight: 378.492
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 81118-43-6.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-decylthio-N-methyl-5-nitrophthalimide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-decylthio-N-methyl-5-nitrophthalimide(81118-43-6)
    11. EPA Substance Registry System: 3-decylthio-N-methyl-5-nitrophthalimide(81118-43-6)

  • 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: 81118-43-6(Hazardous Substances Data)

81118-43-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81118-43-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,1,1 and 8 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 81118-43:
(7*8)+(6*1)+(5*1)+(4*1)+(3*8)+(2*4)+(1*3)=106
106 % 10 = 6
So 81118-43-6 is a valid CAS Registry Number.

81118-43-6Upstream product

81118-43-6Downstream Products

81118-43-6Relevant articles and documents

92. Aromatic Nucleophilic Substitution. Part 1. Regiospecific Substitution of the Nitro Groups in 3,5-Dinitrophthalic-Acid Derivatives

Fischer, Walter,Kvita, Vratislav

, p. 846 - 853 (1985)

The regioselectivity of nucleophilic substitution of the nitro groups in 3,5-dinitrophthalic anhydrides and 3,5-dinitrophthalimides (Scheme) with a variety of nucleophiles (Nu(1-)) was studied.In all case, the 3-nitro group was selectively substituted.With excess of the same nucleophilic reagent or with other nucleophiles, the 5-nitro group could subsequently be replaced.

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