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106498-75-3

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106498-75-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106498-75-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,4,9 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 106498-75:
(8*1)+(7*0)+(6*6)+(5*4)+(4*9)+(3*8)+(2*7)+(1*5)=143
143 % 10 = 3
So 106498-75-3 is a valid CAS Registry Number.

106498-75-3Relevant articles and documents

Catalytic performance of bulk and colloidal Co/Al layered double hydroxide with Au nanoparticles in aerobic olefin oxidation

Leandro, Sónia R.,Fernandes, Cristina I.,Viana,Mourato,Vaz, Pedro D.,Nunes, Carla D.

, (2019)

A Co/Al layered double hydroxide material was synthesized in both bulk and exfoliated (colloidal) forms. Anion exchange with methionine allowed immobilization of Au nanoparticles previously prepared by a biomimetic method using an anti-oxidant tea aqueous extract to reduce the Au salt solution. The catalytic performance of bulk and exfoliated clays Au-hybrid materials was assessed in aerobic olefin epoxidation. Both catalysts were very active towards the epoxide products and with very interesting substrate conversion levels after 80 h reaction time. The Au-exfoliated material, where the nanosheets work as large ligands, yielded higher product stereoselectivity in the case of limonene epoxidation. This arises from a confined environment around the Au nanoparticles wrapped by the clay nanosheets modulating access to the catalytic active centres by reagents. Mechanistic assessment was also accomplished for styrene oxidation by DFT methods.

Microwave-assisted oxidation of saturated and unsaturated alcohols with t-butyl hydroperoxide and zeolites

Palombi, Laura,Bonadiesa, Francesco,Scettri, Arrigo

, p. 15867 - 15876 (2007/10/03)

Under microwave irradiation 3? molecular sieves promote the oxidation of secondary (linear and cyclic) and benzylic alcohols to the corresponding carbonyl compounds by t-butyl hydroperoxide. Under the same conditions, α,β-unsaturated alcohols are converted into α,β-epoxyalcohols in regio- and diastereoselective way. Both oxidative processes can be performed under solvent-free conditions; however, epoxidation of allylic alcohols is found to proceed with more satisfactory efficiency in saturated aliphatic hydrocarbon (n-hexane or cyclohexane).

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