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1412908-27-0

N-trifluoroacetyl-(S)-phenylalanyl-glycyl-(S)-N-methyl-leucineanilide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • N-trifluoroacetyl-(S)-phenylalanyl-glycyl-(S)-N-methyl-leucineanilide

    Cas No: 1412908-27-0

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  • 1412908-27-0 Structure

  • Basic information

    1. Product Name: N-trifluoroacetyl-(S)-phenylalanyl-glycyl-(S)-N-methyl-leucineanilide
    2. Synonyms: N-trifluoroacetyl-(S)-phenylalanyl-glycyl-(S)-N-methyl-leucineanilide
    3. CAS NO:1412908-27-0
    4. Molecular Formula:
    5. Molecular Weight: 520.552
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1412908-27-0.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-trifluoroacetyl-(S)-phenylalanyl-glycyl-(S)-N-methyl-leucineanilide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-trifluoroacetyl-(S)-phenylalanyl-glycyl-(S)-N-methyl-leucineanilide(1412908-27-0)
    11. EPA Substance Registry System: N-trifluoroacetyl-(S)-phenylalanyl-glycyl-(S)-N-methyl-leucineanilide(1412908-27-0)

  • 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: 1412908-27-0(Hazardous Substances Data)

1412908-27-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1412908-27-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,2,9,0 and 8 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1412908-27:
(9*1)+(8*4)+(7*1)+(6*2)+(5*9)+(4*0)+(3*8)+(2*2)+(1*7)=140
140 % 10 = 0
So 1412908-27-0 is a valid CAS Registry Number.

1412908-27-0Relevant articles and documents

Selective peptide modifications via ruthenium-catalyzed allylic alkylations

Bayer, Anton,Kazmaier, Uli

, p. 8491 - 8497 (2014)

Ruthenium-catalyzed allylic alkylations are an interesting alternative to palladium-catalyzed processes, since they can provide products which are not accessible under Pd-catalysis. Chiral terminal allylic substrates can be reacted with perfect stereo- and regioretention, and also (Z)-configured allylic substrates can be converted isomerization-free. This allows highly stereoselective modifications of peptides at glycine subunits. The configuration at the α-position of the new generated α-amino acid can be controlled by the chiral peptide chain, and at the β-position by using chiral allylic substrates.

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