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2,2-dideuterio-1-phenyl-1,3-butanedione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

10573-29-2

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10573-29-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10573-29-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,7 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 10573-29:
(7*1)+(6*0)+(5*5)+(4*7)+(3*3)+(2*2)+(1*9)=82
82 % 10 = 2
So 10573-29-2 is a valid CAS Registry Number.

10573-29-2Upstream product

10573-29-2Downstream Products

10573-29-2Relevant academic research and scientific papers

The low-barrier hydrogen bond of deuterated benzoylacetone probed by very low temperature neutron and X-ray diffraction studies and theoretical calculations

Madsen, Georg K. H.,McIntyre, Garry J.,Schiott, Birgit,Larsen, Finn K.

, p. 5539 - 5547 (2007)

Low-temperature neutron diffraction data is used to show that the enol deuteron in deuterated benzoylacetone has a bimodal probability density distribution. In a previous study of normal benzoylacetone we showed that the enol hydrogen atom has a broad unimodal probability density distribution. Deuteration gives hardly any change to the molecular framework other than a small lengthening of the O...O distance. We solve the vibrational Hamiltonian for a series of model hydrogen potentials and show how the proton/deuteron probability density function can become strongly perturbed by small changes to the potential. The potentials are used to show that the deuteron in benzoylacetonc can be interpreted as an atom tunnelling between two possible localised positions, while the proton in benzoylacetone can be viewed as having sufficient energy to shuttle over the low-energy barrier, even at 15 K. We underline the necessity of accounting for the dynamic nature of the hydrogen bond and not relying on a description of the proton/ deuteron by a single atomic coordinate, and compare our results to structure correlation studies.

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