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CAS

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623549-61-1

N-[6-(2,2,2-trifluoroacetylamino)cyclohex-3-enyl]-2,2,2-trifluoroacetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 623549-61-1 Structure

  • Basic information

    1. Product Name: N-[6-(2,2,2-trifluoroacetylamino)cyclohex-3-enyl]-2,2,2-trifluoroacetamide
    2. Synonyms: N-[6-(2,2,2-trifluoroacetylamino)cyclohex-3-enyl]-2,2,2-trifluoroacetamide
    3. CAS NO:623549-61-1
    4. Molecular Formula:
    5. Molecular Weight: 304.192
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 623549-61-1.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-[6-(2,2,2-trifluoroacetylamino)cyclohex-3-enyl]-2,2,2-trifluoroacetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-[6-(2,2,2-trifluoroacetylamino)cyclohex-3-enyl]-2,2,2-trifluoroacetamide(623549-61-1)
    11. EPA Substance Registry System: N-[6-(2,2,2-trifluoroacetylamino)cyclohex-3-enyl]-2,2,2-trifluoroacetamide(623549-61-1)

  • 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: 623549-61-1(Hazardous Substances Data)

623549-61-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 623549-61-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,3,5,4 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 623549-61:
(8*6)+(7*2)+(6*3)+(5*5)+(4*4)+(3*9)+(2*6)+(1*1)=161
161 % 10 = 1
So 623549-61-1 is a valid CAS Registry Number.

623549-61-1Downstream Products

623549-61-1Relevant articles and documents

Scope of the directed dihydroxylation: Application to cyclic homoallylic alcohols and trihaloacetamides

Donohoe, Timothy J.,Mitchell, Lee,Waring, Michael J.,Helliwell, Madeleine,Bell, Andrew,Newcombe, Nicholas J.

, p. 2173 - 2186 (2007/10/03)

The synthesis and directed dihydroxylation of a range of cyclic alkenes was investigated. Both homoallylic alcohols and homoallylic trihaloacetamides were found to be efficient directing groups, giving rise to good to excellent levels of remote asymmetric induction with OsO4-TMEDA. Interestingly, in all cases examined, trifluoroacetamides were found to be superior to trichloroacetamides as directing groups and an argument is presented which rationalises this observation.

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