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2,2,6,6-d4-4-tert.-Butylmethylencyclohexan, also known as deuterated 4-tert-butylmethylcyclohexane, is a chemical compound that is a derivative of cyclohexane. It characterized is by the presence of a tert-butyl group (a methyl group attached to a tertiary carbon) and a methyl group attached to the cyclohexane ring. The compound is deuterated, meaning it contains four deuterium atoms (an isotope of hydrogen with one proton and one neutron) in place of regular hydrogen atoms. This deuteration can be used to study the compound's properties and reactions, as deuterium atoms have different mass and chemical behavior compared to regular hydrogen atoms. The compound is often used in scientific research and chemical analysis, particularly in the field of organic chemistry and spectroscopy, to investigate the effects of isotopic substitution on molecular properties and reaction mechanisms.

54789-06-9

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54789-06-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54789-06-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,7,8 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 54789-06:
(7*5)+(6*4)+(5*7)+(4*8)+(3*9)+(2*0)+(1*6)=159
159 % 10 = 9
So 54789-06-9 is a valid CAS Registry Number.

54789-06-9Downstream Products

54789-06-9Relevant academic research and scientific papers

Visible-Light Controlled Divergent Catalysis Using a Bench-Stable Cobalt(I) Hydride Complex

Beltran, Frédéric,Bergamaschi, Enrico,Teskey, Christopher J.

supporting information, p. 5180 - 5184 (2020/04/22)

While the use of visible light in conjunction with transition metal catalysis offers powerful opportunities to switch between on/-off states of catalytic activity, the next frontier would be the ability to switch the actual function of the catalyst and resulting products. Here we report such an example of multi-dimensional catalysis. Featuring an easily prepared, bench-stable cobalt(I) hydride complex in conjunction with pinacolborane, we can switch the reaction outcome between two widely employed transformations, olefin migration and hydroboration, with visible light as the trigger.

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