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9-Deuteriophenanthrene is a deuterated derivative of phenanthrene, a polycyclic aromatic hydrocarbon (PAH) consisting of three fused benzene rings. In 9-deuteriophenanthrene, one of the hydrogen atoms at the 9th position of the phenanthrene molecule is replaced by a deuterium atom, which is a stable isotope of hydrogen with one neutron and one proton. This substitution can be used for various purposes, such as studying the chemical and physical properties of phenanthrene, as well as its environmental behavior and potential applications in fields like materials science and organic chemistry. The presence of deuterium can affect the compound's reactivity, stability, and spectroscopic properties, making 9-deuteriophenanthrene a valuable tool for research and analysis.

4819-99-2

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4819-99-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4819-99-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,1 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4819-99:
(6*4)+(5*8)+(4*1)+(3*9)+(2*9)+(1*9)=122
122 % 10 = 2
So 4819-99-2 is a valid CAS Registry Number.

4819-99-2Downstream Products

4819-99-2Relevant academic research and scientific papers

Visible-light-induced photocatalytic reductive transformations of organohalides

Kim, Hyejin,Lee, Chulbom

supporting information, p. 12303 - 12306 (2013/02/23)

A photo opportunity: A visible-light-excited iridium catalyst delivers electrons from an amine to an organohalide. The electron transfer then induces reductive scission of the carbon-halogen bond, generating the corresponding alkyl, alkenyl, and aryl radical that can undergo cyclization and hydrodehalogenation reactions. Copyright

Hydrogen Transfer Reactions, 6. Dehydrogenation of 1,2-Dihydroarenes by Quinones: Regio- and Stereoselectivity in the Two-Step Mechanism

Paukstat, Ralf,Brock, Martin,Heesing, Albert

, p. 2579 - 2592 (2007/10/02)

1,2-Dihydronaphthalene (1) is dehydrogenated by o- and p-quinones in a two-step mechanism.In the rate determining step a hydride ion is abstracted from the 2-position by o-chloro- (4a) and o-bromoanil (4b) with high regioselectivity.Ion pairing leads to highly stereoselective cis-elimination of the proton.Stereoselectivity, primary isotope effects, and activation entropy are consistent with a coplanar coordination in the transition state and participation of tunneling. p-Quinones show different regioselectivity in the hydride abstraction step.The dehydrogenation of 9,10-dihydrophenanthrene (3) proceeds in a similar way.

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