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891195-01-0

N-Boc-L-Phe-L-Leu-L-Ala-3-acetylenephenylamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 891195-01-0 Structure

  • Basic information

    1. Product Name: N-Boc-L-Phe-L-Leu-L-Ala-3-acetylenephenylamide
    2. Synonyms: N-Boc-L-Phe-L-Leu-L-Ala-3-acetylenephenylamide
    3. CAS NO:891195-01-0
    4. Molecular Formula:
    5. Molecular Weight: 548.682
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 891195-01-0.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-Boc-L-Phe-L-Leu-L-Ala-3-acetylenephenylamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-Boc-L-Phe-L-Leu-L-Ala-3-acetylenephenylamide(891195-01-0)
    11. EPA Substance Registry System: N-Boc-L-Phe-L-Leu-L-Ala-3-acetylenephenylamide(891195-01-0)

  • 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: 891195-01-0(Hazardous Substances Data)

891195-01-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 891195-01-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,1,1,9 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 891195-01:
(8*8)+(7*9)+(6*1)+(5*1)+(4*9)+(3*5)+(2*0)+(1*1)=190
190 % 10 = 0
So 891195-01-0 is a valid CAS Registry Number.

891195-01-0Relevant articles and documents

Synthesis of cyclic peptides using a palladium-catalyzed enyne cycloisomerization

Balraju,Dev, R. Vasu,Reddy, D. Srinivasa,Iqbal, Javed

, p. 3569 - 3571 (2007/10/03)

In this letter, we report a palladium-catalyzed enyne cycloisomerization of linear peptides to generate small cyclic peptides embedded with a conjugated 1,3-diene. The utility of these resulting macrocyclic dienes is demonstrated by carrying out [4+2] cyc

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