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1417862-50-0

N,N′-[1,4-phenylenebis(iminocarbonyl)]di(L-phenylalanine) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1417862-50-0 Structure

  • Basic information

    1. Product Name: N,N′-[1,4-phenylenebis(iminocarbonyl)]di(L-phenylalanine)
    2. Synonyms: N,N′-[1,4-phenylenebis(iminocarbonyl)]di(L-phenylalanine)
    3. CAS NO:1417862-50-0
    4. Molecular Formula:
    5. Molecular Weight: 490.516
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1417862-50-0.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,N′-[1,4-phenylenebis(iminocarbonyl)]di(L-phenylalanine)(CAS DataBase Reference)
    10. NIST Chemistry Reference: N,N′-[1,4-phenylenebis(iminocarbonyl)]di(L-phenylalanine)(1417862-50-0)
    11. EPA Substance Registry System: N,N′-[1,4-phenylenebis(iminocarbonyl)]di(L-phenylalanine)(1417862-50-0)

  • 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: 1417862-50-0(Hazardous Substances Data)

1417862-50-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1417862-50-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,7,8,6 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1417862-50:
(9*1)+(8*4)+(7*1)+(6*7)+(5*8)+(4*6)+(3*2)+(2*5)+(1*0)=170
170 % 10 = 0
So 1417862-50-0 is a valid CAS Registry Number.

1417862-50-0Downstream Products

1417862-50-0Relevant articles and documents

Synthesis and UV/Vis analysis of amino acid-derived bisurea-type receptors involving anion complexation

Stapf, Manuel,Seichter, Wilhelm,Weber, Edwin

, p. 409 - 419 (2015)

Sixteen new bisurea compounds incorporating versatile proteinogenic amino acids as well as nipecotic acid have been synthesized via addition reaction to aryl diisocyanates. The products were analytically characterized and their ability for anion recognition was studied by UV/Vis spectroscopy. In the presence of fluoride, acetate or dihydrogenphosphate ions, hyperchromic and bathochromic peak shifts were determined. By way of contrast, bromide, iodide, or hydrogensulfate ions cause no significant change of absorbance. The special effect of heterocyclic derivatives was explained by molecular modeling calculations. In addition, the crystal structure of the byproduct dimethyl N,N′-(1,4-phenylene)dicarbamate is discussed.

Synthesis of the bifunctional ligand N,N'-[1,4-phenylenebis(iminocarbonyl)] di(L-phenylalanine) and crystal structure of its supramolecular coordination polymer with lead(II)

Stapf, Manuel,Boehle, Tony,Seichter, Wilhelm,Mertens, Florian O. R. L.,Weber, Edwin

, p. 1166 - 1172 (2013/01/15)

The new linker-type ligand 1, featuring two L-phenylalanine-terminated urea moieties attached to the para positions of a central phenylene unit has been synthesized. Its coordination polymer formed with lead(II) and containing DMF and water as solvent mol

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