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N-cyclohexyl-exo-5,6-epoxybicyclo[2.2.1]heptan-endo,endo-2,3-dicarboximide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1235470-50-4 Structure
  • Basic information

    1. Product Name: N-cyclohexyl-exo-5,6-epoxybicyclo[2.2.1]heptan-endo,endo-2,3-dicarboximide
    2. Synonyms: N-cyclohexyl-exo-5,6-epoxybicyclo[2.2.1]heptan-endo,endo-2,3-dicarboximide
    3. CAS NO:1235470-50-4
    4. Molecular Formula:
    5. Molecular Weight: 261.321
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1235470-50-4.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-cyclohexyl-exo-5,6-epoxybicyclo[2.2.1]heptan-endo,endo-2,3-dicarboximide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-cyclohexyl-exo-5,6-epoxybicyclo[2.2.1]heptan-endo,endo-2,3-dicarboximide(1235470-50-4)
    11. EPA Substance Registry System: N-cyclohexyl-exo-5,6-epoxybicyclo[2.2.1]heptan-endo,endo-2,3-dicarboximide(1235470-50-4)
  • 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: 1235470-50-4(Hazardous Substances Data)

1235470-50-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1235470-50-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,5,4,7 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1235470-50:
(9*1)+(8*2)+(7*3)+(6*5)+(5*4)+(4*7)+(3*0)+(2*5)+(1*0)=134
134 % 10 = 4
So 1235470-50-4 is a valid CAS Registry Number.

1235470-50-4Downstream Products

1235470-50-4Relevant articles and documents

Ethanolysis of N-substituted norbornane epoxyimides: Discovery of diverse pathways depending on substituent's character

Petrova, Tetyana,Tarabara, Igor,Palchikov, Vitaliy,Kasyan, Liliya,Kosenkov, Dmytro,Okovytyy, Sergiy,Gorb, Leonid,Shishkina, Svetlana,Shishkin, Oleg,Leszczynski, Jerzy

experimental part, p. 2142 - 2157 (2010/07/04)

Combined experimental and theoretical studies have been carried out to investigate the transformations of the epoxyimides of norbornane into heterocyclic compounds. We established that interaction of the aryl-substituted epoxyimides of norbornane with sod

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