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Cu(L-glycine) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 15488-81-0 Structure
  • Basic information

    1. Product Name: Cu(L-glycine)
    2. Synonyms:
    3. CAS NO:15488-81-0
    4. Molecular Formula:
    5. Molecular Weight: 137.605
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 15488-81-0.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: Cu(L-glycine)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cu(L-glycine)(15488-81-0)
    11. EPA Substance Registry System: Cu(L-glycine)(15488-81-0)
  • 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: 15488-81-0(Hazardous Substances Data)

15488-81-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15488-81-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,8 and 8 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 15488-81:
(7*1)+(6*5)+(5*4)+(4*8)+(3*8)+(2*8)+(1*1)=130
130 % 10 = 0
So 15488-81-0 is a valid CAS Registry Number.

15488-81-0Upstream product

15488-81-0Downstream Products

15488-81-0Relevant articles and documents

TERNARY MIXED-LIGAND COPPER(II) COMPLEXES WITH CHIRAL AMINOPHOSPHONIC ACIDS AND AMINO ACIDS

Nabirkina, E. P.,Ignat'eva, T. I.,Raevskii, O. A.,Belov, Yu. P.

, p. 2278 - 2281 (1989)

Ternary mixed-ligand complexes of divalent copper, where one ligand is an α-aminoalkylphosphonic acid (APA) and the second ligand is L-phenylalanine, L-tyrosine, or L-hydroxyphenylalanine, are studied by potentiometric titration in aqueous at 25 deg C and μ=0.1.A maximum in the formation of the ternary complexes is exhibited at pH 7-8.The log Kst for the complexes formed and the statistical parameters characterizing the ternary complexes Δlog K and log X are determined.The effect of substituents on the α-carbon atom of the α-APA and of hydroxy groups on the phenyl substituent of the α-amino acids on the nature of the distribution of the complexes formed is studied.

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