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958892-01-8

N-[(1S)-1-phenyl-ethyl]-2-trifluoromethyl-acrylamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 958892-01-8 Structure

  • Basic information

    1. Product Name: N-[(1S)-1-phenyl-ethyl]-2-trifluoromethyl-acrylamide
    2. Synonyms: N-[(1S)-1-phenyl-ethyl]-2-trifluoromethyl-acrylamide
    3. CAS NO:958892-01-8
    4. Molecular Formula:
    5. Molecular Weight: 243.229
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 958892-01-8.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-[(1S)-1-phenyl-ethyl]-2-trifluoromethyl-acrylamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-[(1S)-1-phenyl-ethyl]-2-trifluoromethyl-acrylamide(958892-01-8)
    11. EPA Substance Registry System: N-[(1S)-1-phenyl-ethyl]-2-trifluoromethyl-acrylamide(958892-01-8)

  • 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: 958892-01-8(Hazardous Substances Data)

958892-01-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 958892-01-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,8,8,9 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 958892-01:
(8*9)+(7*5)+(6*8)+(5*8)+(4*9)+(3*2)+(2*0)+(1*1)=238
238 % 10 = 8
So 958892-01-8 is a valid CAS Registry Number.

958892-01-8Downstream Products

958892-01-8Relevant articles and documents

The role of fluorine in the stereoselective tandem aza-Michael addition to acrylamide acceptors: An experimental and theoretical mechanistic study

Fustero, Santos,Chiva, Gema,Piera, Julio,Volonterio, Alessandro,Zanda, Matteo,Gonzalez, Javier,Ramallal, Antonio Moran

, p. 8530 - 8542 (2007)

Aza-Michael additions of αamino esters to fluorinated acceptors take place in a highly stereoselective manner, to give partially modified ψNHCH2]retropeptides incorporating a hydrolytically stable trifluoroalanine mimic. The reaction mechanism

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