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113366-82-8

Benzenamine, 3,3'-(2,5,8,11-tetraoxadodecane-1,12-diyl)bis[2-methoxy-5-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 113366-82-8 Structure

  • Basic information

    1. Product Name: Benzenamine, 3,3'-(2,5,8,11-tetraoxadodecane-1,12-diyl)bis[2-methoxy-5-methyl-
    2. Synonyms:
    3. CAS NO:113366-82-8
    4. Molecular Formula: C24H36N2O6
    5. Molecular Weight: 448.56
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 113366-82-8.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: Benzenamine, 3,3'-(2,5,8,11-tetraoxadodecane-1,12-diyl)bis[2-methoxy-5-methyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenamine, 3,3'-(2,5,8,11-tetraoxadodecane-1,12-diyl)bis[2-methoxy-5-methyl-(113366-82-8)
    11. EPA Substance Registry System: Benzenamine, 3,3'-(2,5,8,11-tetraoxadodecane-1,12-diyl)bis[2-methoxy-5-methyl-(113366-82-8)

  • 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: 113366-82-8(Hazardous Substances Data)

113366-82-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113366-82-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,3,6 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 113366-82:
(8*1)+(7*1)+(6*3)+(5*3)+(4*6)+(3*6)+(2*8)+(1*2)=108
108 % 10 = 8
So 113366-82-8 is a valid CAS Registry Number.

113366-82-8Relevant articles and documents

SYNTHESIS OF NOVEL CROWN DERIVATIVES INCORPORATING A DIAMINOPHOSPHINE GROUP IN A POLYETHER MACROCYCLE

Dutasta, Jean Pierre,Simon, Pascal

, p. 3577 - 3580 (1987)

The efficient synthesis of 17- to 21-membered ring phosphorus compounds is described.The derivatives incorporate a diaminophosphine group in a polyether macrocycle.

Synthesis and molecular structure of new phosphorous-crown compounds containing the thiophosphoryl group

Declercq, Jean-Paul,Delangle, Pascale,Dutasta, Jean-Pierre,Van Oostenryck, Luc,Simon, Pascal,Tinant, Bernard

, p. 2471 - 2478 (2007/10/03)

The synthesis and characterization of four phosphorus macrocycles (1-4) are reported. The X-ray crystal structures of compounds 1-4 and solvate 1-H2O show the molecules in asymmetric conformations with at least one methyl group of the phenoxy substituants oriented toward the centre of the macrocyclic cavity. Variable-temperature 1H NMR experiments show that in solution the molecules exist mainly as rapidly interconverting conformers. In the 18-membered ring 1, the dynamic process results in the enantiomerization of asymmetric conformers with a barrier of 8 kcal mol-1.? The 21-membered ring 3 is more flexible and exists in several conformations.

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