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159174-83-1

Boc-Leu-Phe-Pro-OMe is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 159174-83-1 Structure

  • Basic information

    1. Product Name: Boc-Leu-Phe-Pro-OMe
    2. Synonyms: Boc-Leu-Phe-Pro-OMe
    3. CAS NO:159174-83-1
    4. Molecular Formula:
    5. Molecular Weight: 489.612
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 159174-83-1.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: Boc-Leu-Phe-Pro-OMe(CAS DataBase Reference)
    10. NIST Chemistry Reference: Boc-Leu-Phe-Pro-OMe(159174-83-1)
    11. EPA Substance Registry System: Boc-Leu-Phe-Pro-OMe(159174-83-1)

  • 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: 159174-83-1(Hazardous Substances Data)

159174-83-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 159174-83-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,1,7 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 159174-83:
(8*1)+(7*5)+(6*9)+(5*1)+(4*7)+(3*4)+(2*8)+(1*3)=161
161 % 10 = 1
So 159174-83-1 is a valid CAS Registry Number.

159174-83-1Relevant articles and documents

Efficient construction of proline-containing β-turn mimetic cyclic tetrapeptides via CuAAC macrocyclization

Chouhan, Gagan,James, Keith

supporting information, p. 1206 - 1209 (2013/05/21)

A range of macrocyclic β-turn mimetic tetrapeptides was prepared by efficient copper-tris(triazole) ligand complex catalyzed azide-alkyne "click" macrocyclizations in good to high yields. Preliminary conformational studies using X-ray crystallography and NMR spectroscopy demonstrated the presence of intramolecular H-bonds characteristic of β-turns in these cyclic tetrapeptides.

A Cyclic Analogue of Hexapeptide Tyr-Val-Pro-Leu-Phe-Pro, A Peptide Immunostimulant

Siemion, I. Z.,Szewczuk, Z.,Lisowski, M.

, p. 877 - 883 (2007/10/02)

A cyclic analogue of the peptide immunoeffector, hexapeptide Tyr-Val-Pro-Leu-Phe-Pro, was synthesized by different methods in solution.A comparison of the BOP reagent with the classical p-nitrophenyl ester method for the cyclization reaction shows that in

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