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CAS

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162355-99-9

N-Cyclohex-1-enyl-N-((E)-1-methyl-but-2-enyl)-isobutyramide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 162355-99-9 Structure

  • Basic information

    1. Product Name: N-Cyclohex-1-enyl-N-((E)-1-methyl-but-2-enyl)-isobutyramide
    2. Synonyms: N-Cyclohex-1-enyl-N-((E)-1-methyl-but-2-enyl)-isobutyramide
    3. CAS NO:162355-99-9
    4. Molecular Formula:
    5. Molecular Weight: 235.37
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 162355-99-9.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-Cyclohex-1-enyl-N-((E)-1-methyl-but-2-enyl)-isobutyramide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-Cyclohex-1-enyl-N-((E)-1-methyl-but-2-enyl)-isobutyramide(162355-99-9)
    11. EPA Substance Registry System: N-Cyclohex-1-enyl-N-((E)-1-methyl-but-2-enyl)-isobutyramide(162355-99-9)

  • 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: 162355-99-9(Hazardous Substances Data)

162355-99-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 162355-99-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,3,5 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 162355-99:
(8*1)+(7*6)+(6*2)+(5*3)+(4*5)+(3*5)+(2*9)+(1*9)=139
139 % 10 = 9
So 162355-99-9 is a valid CAS Registry Number.

162355-99-9Relevant articles and documents

Stereochemical consequences of the Lewis acid-promoted 3-aza-cope rearrangement of N-alkyl-N-allyl enamines

Cook, Ggregory R.,Stille, John R.

, p. 4105 - 4124 (1994)

Internal and relative asymmetric induction were examined for the electrophile promoted 3-aza-Cope rearrangement of substituted N-alkyl-N-allyl enamines. In general, internal asymmetric induction was highly variable, and was dependent both upon the nature

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