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632326-60-4

4-Pentenamide, N-[3-(trifluoromethyl)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 632326-60-4 Structure

  • Basic information

    1. Product Name: 4-Pentenamide, N-[3-(trifluoromethyl)phenyl]-
    2. Synonyms:
    3. CAS NO:632326-60-4
    4. Molecular Formula: C12H12F3NO
    5. Molecular Weight: 243.229
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 632326-60-4.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: 4-Pentenamide, N-[3-(trifluoromethyl)phenyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-Pentenamide, N-[3-(trifluoromethyl)phenyl]-(632326-60-4)
    11. EPA Substance Registry System: 4-Pentenamide, N-[3-(trifluoromethyl)phenyl]-(632326-60-4)

  • 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: 632326-60-4(Hazardous Substances Data)

632326-60-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 632326-60-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,2,3,2 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 632326-60:
(8*6)+(7*3)+(6*2)+(5*3)+(4*2)+(3*6)+(2*6)+(1*0)=134
134 % 10 = 4
So 632326-60-4 is a valid CAS Registry Number.

632326-60-4Relevant articles and documents

Enantioselective Synthesis of Cyclic Secondary Amines through Mo-Catalyzed Asymmetric Ring-Closing Metathesis (ARCM)

Dolman, Sarah J.,Schrock, Richard R.,Hoveyda, Amir H.

, p. 4899 - 4902 (2003)

(Equation Presented) Carboyclic amines are synthesized efficiently in up to 93% ee by asymmetric ring-closing metathesis (ARCM) with 2-5 mol % chiral Mo complexes. An example is provided where the catalyst is prepared in situ (catalyst isolation not neede

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