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1404310-13-9

Z-GABA-Gly-OtBu is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1404310-13-9 Structure

  • Basic information

    1. Product Name: Z-GABA-Gly-OtBu
    2. Synonyms: Z-GABA-Gly-OtBu
    3. CAS NO:1404310-13-9
    4. Molecular Formula:
    5. Molecular Weight: 350.415
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1404310-13-9.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: Z-GABA-Gly-OtBu(CAS DataBase Reference)
    10. NIST Chemistry Reference: Z-GABA-Gly-OtBu(1404310-13-9)
    11. EPA Substance Registry System: Z-GABA-Gly-OtBu(1404310-13-9)

  • 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: 1404310-13-9(Hazardous Substances Data)

1404310-13-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1404310-13-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,4,3,1 and 0 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1404310-13:
(9*1)+(8*4)+(7*0)+(6*4)+(5*3)+(4*1)+(3*0)+(2*1)+(1*3)=89
89 % 10 = 9
So 1404310-13-9 is a valid CAS Registry Number.

1404310-13-9Relevant articles and documents

An approach to nanobioparticles - Synthesis and characterization of fulleropeptides

Bjelakovic, Mira,Todorovic, Nina,Milic, Dragana

, p. 5291 - 5300 (2012)

Two sets of new peptides incorporating fulleropyrrolidine units - Fp-GABAn-Glym-OtBu - have been designed, synthesized and completely characterized. In the first series the chain contained only GABA (γ-aminobutyric) residues, whereas in the second one glycine moieties were also inserted as well as GABA. Most of the target compounds were prepared by DCC/DMAP-assisted coupling of previously synthesized GABA-containing fulleropyrrolidinic acid and corresponding C-protected small peptides, although for two fulleropeptides [3+2] cycloadditions of azomethine ylides to C 60 were employed. All new compounds were characterized by standard spectroscopic methods. Complete assignments of peptide spin systems were achieved by extensive NMR analysis (1H, 13C, H,H-COSY, HSQC, HMBC and TOCSY). Copyright

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