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Aluminum, (hydroxytriphenylstannanato)bis(2-propanolato)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 138977-01-2 Structure
  • Basic information

    1. Product Name: Aluminum, (hydroxytriphenylstannanato)bis(2-propanolato)-
    2. Synonyms:
    3. CAS NO:138977-01-2
    4. Molecular Formula: C24H29AlO3Sn
    5. Molecular Weight: 511.184
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 138977-01-2.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: Aluminum, (hydroxytriphenylstannanato)bis(2-propanolato)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Aluminum, (hydroxytriphenylstannanato)bis(2-propanolato)-(138977-01-2)
    11. EPA Substance Registry System: Aluminum, (hydroxytriphenylstannanato)bis(2-propanolato)-(138977-01-2)
  • 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: 138977-01-2(Hazardous Substances Data)

138977-01-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138977-01-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,9,7 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 138977-01:
(8*1)+(7*3)+(6*8)+(5*9)+(4*7)+(3*7)+(2*0)+(1*1)=172
172 % 10 = 2
So 138977-01-2 is a valid CAS Registry Number.

138977-01-2Downstream Products

138977-01-2Relevant articles and documents

Some new organotin(IV), aluminium(III)-μ-oxoisopropoxides and their benzoylacetone derivatives

Kapoor, Pramesh N.,Bhagi, Ajay K.,Kapoor, Ramesh N.,Sharma, Harish K.

, p. 321 - 325 (1991)

The first organotin(IV), aluminium(III)-μ-oxoisopropoxides of the type iPr)2 (R = Me or Ph) have been made by heating of trimethyl- or triphenyl-tin acetate with aluminium isopropoxide.The reactions of these μ-oxoisopropoxides with be

Organometallic assemblies: π-electron delocalization, μ-bridging spacers, flexibility, lipophilic nature, bio-accessibility, bioavailability, intracellular trafficking pathways and antimicrobial assimilation

Kumar, Rajiv,Chhikara, Bhupender S.

, p. 64 - 76 (2015)

Supramolecular architectures of triphenylSn(IV)-A(lII)-μ-oxoisopropoxide (organometallic assemblies i.e. Ph3SnOAl(OPri)L and Ph3SnOAl(L)2) were yielded by the reaction of triphenyltin acetate, aluminiumisopropoxide and different ligands (L1 to L5) having different backbones (NOONO and OONO) in presence of xylene. Spectral analysis (IR, 1H NMR, 13C NMR, 27Al NMR, 119Sn NMR and MS) and molecular modeling revealed coordination modes between metals and donor atoms entirely within supramolecular architectures. Ph3SnOAl(OPri)L and Ph3SnOAl(L)2 showed tetra- and penta-coordination of metals center with distorted tetrahedral and distorted trigonal-bipyramidal geometries for Sn(IV) and Al(III) respectively. Organometallic assemblies went through self-organization of atoms through μ-bridging, hydrophobic, hydrophilic and electrostatic effects. Antimicrobial assimilation was dependent on good adsorptive ability, generated by the interaction between microbial and organometallic assemblies. Finally, organometallic assemblies were screened extensively in-vitro against a number of pathogens. The toxicity of metal ion(s) was reduced or eliminated by changing donor backbone of ligands. Computational models and molecular mechanics were employed to reveal architectural features. The donating nature of substituent of ligands affected antimicrobial assimilation. Because of this, desired modifications were done through computational calculations to achieve perfect organometallic assemblies with HOMO for ligands(L1 to L5).

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