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  • 232279-44-6 Structure
  • Basic information

    1. Product Name: Trp-Aib-Gly-Leu-NHPh
    2. Synonyms: Trp-Aib-Gly-Leu-NHPh
    3. CAS NO:232279-44-6
    4. Molecular Formula:
    5. Molecular Weight: 534.659
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 232279-44-6.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: Trp-Aib-Gly-Leu-NHPh(CAS DataBase Reference)
    10. NIST Chemistry Reference: Trp-Aib-Gly-Leu-NHPh(232279-44-6)
    11. EPA Substance Registry System: Trp-Aib-Gly-Leu-NHPh(232279-44-6)
  • 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: 232279-44-6(Hazardous Substances Data)

232279-44-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 232279-44-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,2,2,7 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 232279-44:
(8*2)+(7*3)+(6*2)+(5*2)+(4*7)+(3*9)+(2*4)+(1*4)=126
126 % 10 = 6
So 232279-44-6 is a valid CAS Registry Number.

232279-44-6Downstream Products

232279-44-6Relevant articles and documents

Recognition of quaternary ammonium salts with tetrapeptides containing α-aminoisobutyric acid as a conformational constraint

Yanagihara, Ryoji,Katoh, Masaki,Hanyuu, Masayuki,Miyazawa, Toshifumi,Yamada, Takashi

, p. 551 - 556 (2007/10/03)

Tetrapeptides Trp-Aib-Gly-Leu-NH-Ar (Aib:α-aminoisobutyric acid, 2-amino-2-methylpropanoic acid, Ar = phenyl or 3,5-dimethylphenyl) were synthesized. The peptides bound quaternary ammonium salts as guests in CDCl3. For every guest, the binding constant K of the peptide host which has a 3,5-dimethylphenyl group was larger than that of the host which has a phenyl group. ROESY analysis of the complex revealed that the N+-CH3 groups of the guests were close to the aromatic moieties of the host in the complex. The charge in cation guests, the φ-basicity of the host, and the turn conformation of the peptides were important factors for the complexation.

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