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1,3-Benzenedicarboxamide, 5-(1,1-dimethylethyl)-N,N'-bis[2-(4-hydroxyphenoxy)ethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 849052-75-1 Structure
  • Basic information

    1. Product Name: 1,3-Benzenedicarboxamide, 5-(1,1-dimethylethyl)-N,N'-bis[2-(4-hydroxyphenoxy)ethyl]-
    2. Synonyms:
    3. CAS NO:849052-75-1
    4. Molecular Formula: C28H32N2O6
    5. Molecular Weight: 492.572
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 849052-75-1.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: 1,3-Benzenedicarboxamide, 5-(1,1-dimethylethyl)-N,N'-bis[2-(4-hydroxyphenoxy)ethyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,3-Benzenedicarboxamide, 5-(1,1-dimethylethyl)-N,N'-bis[2-(4-hydroxyphenoxy)ethyl]-(849052-75-1)
    11. EPA Substance Registry System: 1,3-Benzenedicarboxamide, 5-(1,1-dimethylethyl)-N,N'-bis[2-(4-hydroxyphenoxy)ethyl]-(849052-75-1)
  • 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: 849052-75-1(Hazardous Substances Data)

849052-75-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 849052-75-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,0,5 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 849052-75:
(8*8)+(7*4)+(6*9)+(5*0)+(4*5)+(3*2)+(2*7)+(1*5)=191
191 % 10 = 1
So 849052-75-1 is a valid CAS Registry Number.

849052-75-1Downstream Products

849052-75-1Relevant articles and documents

Anion-templated assembly of pseudorotaxanes: Importance of anion template, strength of ion-pair thread association, and macrocycle ring size

Sambrook, Mark R.,Beer, Paul D.,Wisner, James A.,Paul, Rowena L.,Cowley, Andrew R.,Szemes, Fridrich,Drew, Michael G. B.

, p. 2292 - 2302 (2005)

A wide range of pseudorotaxane assemblies containing positively charged pyridinium, pyridinium nicotinamide, imidazolium, benzimidazolium and guanidinium threading components, and macrocyclic isophthalamide polyether ligands have been prepared using a general anion templation procedure. In noncompetitive solvent media, coupling halide anion recognition by a macrocyclic ligand with ion-pairing between the halide anion and a strongly associated cation provides the driving force for interpenetration. Extensive solution 1H NMR binding studies, thermodynamic investigations, and single-crystal X-ray structure determinations reveal that the nature of the halide anion template, strength of the ion-pairing between the anion template and the cationic threading component, and to a lesser extent favorable second sphere π-π aromatic stacking interactions between the positively charged threading component and macrocyclic ligand, together with macrocyclic ring size, affect the efficacy of pseudorotaxane formation.

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