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759457-76-6

N-isobornylaniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 759457-76-6 Structure

  • Basic information

    1. Product Name: N-isobornylaniline
    2. Synonyms: N-isobornylaniline
    3. CAS NO:759457-76-6
    4. Molecular Formula:
    5. Molecular Weight: 229.365
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 759457-76-6.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: N-isobornylaniline(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-isobornylaniline(759457-76-6)
    11. EPA Substance Registry System: N-isobornylaniline(759457-76-6)

  • 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: 759457-76-6(Hazardous Substances Data)

759457-76-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 759457-76-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,9,4,5 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 759457-76:
(8*7)+(7*5)+(6*9)+(5*4)+(4*5)+(3*7)+(2*7)+(1*6)=226
226 % 10 = 6
So 759457-76-6 is a valid CAS Registry Number.

759457-76-6Relevant articles and documents

Amines as Dehalogenating Agents. IV. Hydrocarbons, N-Bornyl- and N-Isobornylaniline Formation in the Reaction between 3-Bromocamphor and N-Methylaniline

Giumanini, Angelo G.,Musiani, Marco M.

, p. 423 - 428 (2007/10/02)

N-Methylanilin (4) reagiert bei 200 deg C im Vergleich zu N,N-Dimethylanilin entweder mit 3-Bromcamphor (2) oder Camphor (3) zu den Kohlenwasserstoffen, Camphen 5 und Tricyclen 6 und N-Bornylanilin (exo-endo-Isomers 7).Bei der Reaktion mit 3 ist Saeurekatalyse notwenig.Untersuchungen zum Mechanismus erlauben es, anzunehmen, dass Camphoranil 8 ein gemeinsames Zwischenprodukt fuer alle Produkte und 4 der H-Donator in den Reduktionsstufen ist, auf der Grundlage von kinetischen und stereochemischen Beweisen und unabhaengigen chemischen Experimenten.

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