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70264-96-9

N-methylcyclohexane-1,1-dicarboximide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 70264-96-9 Structure

  • Basic information

    1. Product Name: N-methylcyclohexane-1,1-dicarboximide
    2. Synonyms: N-methylcyclohexane-1,1-dicarboximide
    3. CAS NO:70264-96-9
    4. Molecular Formula:
    5. Molecular Weight: 167.208
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 70264-96-9.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: N-methylcyclohexane-1,1-dicarboximide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-methylcyclohexane-1,1-dicarboximide(70264-96-9)
    11. EPA Substance Registry System: N-methylcyclohexane-1,1-dicarboximide(70264-96-9)

  • 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: 70264-96-9(Hazardous Substances Data)

70264-96-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70264-96-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,2,6 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 70264-96:
(7*7)+(6*0)+(5*2)+(4*6)+(3*4)+(2*9)+(1*6)=119
119 % 10 = 9
So 70264-96-9 is a valid CAS Registry Number.

70264-96-9Relevant articles and documents

Photochemistry of Aliphatic Imides. Synthesis of Azetidine-2,4-diones via Photochemical Isomerization of Succinimides and N-Formyl-N-methyl α, β -Unsaturated Amides

Maruyama, Kazuhiro,Ishitoku, Takeshi,Kubo, Yasuo

, p. 27 - 34 (2007/10/02)

Photochemical reactions of alkyl-substituted succinimides and N-formyl-N-methyl α, β -unsaturated amides were studied.Photolysis of succinimide 1 gave azetidine-2,4-dione 2 together with a small amount of 3.The photoinduced ring-contraction reaction is explained in terms of a two-photon mechanism.Similarly, several other succinimide derivates photochemically gave the corresponding azetidine-2,4-diones.In addition, the photochemical cyclization of 3 to 2 was extended to the synthesis of azetidine-2,4-diones from N-formyl-N-methyl α, β -unsaturated amides.

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