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  • 1032942-75-8 Structure
  • Basic information

    1. Product Name: C22H26O6
    2. Synonyms:
    3. CAS NO:1032942-75-8
    4. Molecular Formula:
    5. Molecular Weight: 386.445
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1032942-75-8.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: C22H26O6(CAS DataBase Reference)
    10. NIST Chemistry Reference: C22H26O6(1032942-75-8)
    11. EPA Substance Registry System: C22H26O6(1032942-75-8)
  • 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: 1032942-75-8(Hazardous Substances Data)

1032942-75-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1032942-75-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,2,9,4 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1032942-75:
(9*1)+(8*0)+(7*3)+(6*2)+(5*9)+(4*4)+(3*2)+(2*7)+(1*5)=128
128 % 10 = 8
So 1032942-75-8 is a valid CAS Registry Number.

1032942-75-8Relevant articles and documents

Enantiospecific syntheses of copper cubanes, double-stranded copper/palladium helicates, and a (dilithium)-dinkkel coronate from enantiomerically pure bis-1,3-diketones - solid-state self-organization towards wirelike copper/palladium strands

Saalfrank, Rolf W.,Spitzlei, Christine,Scheurer, Andreas,Maid, Harald,Heinemann, Frank W.,Hampel, Frank

experimental part, p. 1472 - 1481 (2009/04/04)

Enantiomerically pure, vicinal diols 1 afforded in a two-step synthesis (etherification and subsequent Claisen condensation) chiral bis-1,3-diketones H2L(S,S) (3a-c) with different substitution patterns. Reaction of these C2-symmetric ligands with various transition-metal acetates in the presence of alkali ions generated distinct polynuclear aggregates 4-8 by diastereoselective self-assembly. Starting from copper(II) acetate monohydrate and depending on the ratio of transitionmetal ion to alkali ion to ligand, chiral tetranuclear copper(II) cubanes (C,C,C,C)-[Cu 4(L(SS)2(OMe)4] (4a-c) or dinuclear copper(II) helicates (P)-[Cu2(L(S,S)2] (5) could be synthesized with square-pyramidal and squareplanar coordination geometry at the metal center. In analogy to the last case, with palladium(II) acetate double-stranded helical systems (F)-[Pd2(L (S,S))2] (6,7) were accessible exhibiting a linear self-organization of ligand-isolated palladium filaments in the solid state with short inter- and intramolecular metal distances. Finally, the introduction of hexacoordinate nickel(II) in combination with lithium hydroxide monohydrate and chiral ligand H2L(S,S) (3 a) allowed the isolation of enantiomerically pure dinuclear nickel(II) coronate [(Li·MeOH) 2C-{(Δ,Λ)-Ni2(L(S,S)) 2(OMe)2}] (8) with two lithium ions in the voids, defined by the oxygen donors in the ligand backbone. The high diastereoselectivity, induced by the chiral ligands, during the self-assembly process in the systems 4-8 could be exemplarily proven by circular dichroism spectroscopy for the synthesized enantiomers of the chiral copper(II) cubane 4a and palladium(II) helicate 6.

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