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

20717-76-4

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20717-76-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20717-76-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,7,1 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 20717-76:
(7*2)+(6*0)+(5*7)+(4*1)+(3*7)+(2*7)+(1*6)=94
94 % 10 = 4
So 20717-76-4 is a valid CAS Registry Number.

20717-76-4Downstream Products

20717-76-4Relevant academic research and scientific papers

Effect of a Hydrogen Pretreatment on the Mechanism of Deuterium Addition Exchange of Propene over Ni-Cu Alloy Catalysts

Naito, Shuichi,Tanimoto, Mitsutoshi

, p. 1253 - 1260 (2007/10/02)

The effects of a hydrogen pretreatment on the activity and reaction intermediate in a C3H6-D2 reaction over a Ni-Cu alloy as well as Ni metal catalysts were investigated in detail by applying an isotope tracer technique.Ni metal and Ni-rich alloy catalysts, cooled down to the reaction temperature under a hydrogen atmosphere (D-surface), exhibited low activity compared to that of a surface evacuated before cooling (E-surface).For Cu-rich alloy catalysts, however, the E-surface exhibited a lower activity and a higher activation energy than did the D-surface.A comparison of the TPF spectra of adsorbed hydrogen with the dependence of the activity upon the evacuation temperature suggests that strongly adsorbed hydrogen retards the reaction over Ni and Ni-rich alloy catalysts at lower temperature.Microwave spectroscopic analysis demonstrated that the reaction intermediates over D- and E-surfaces of Cu-rich alloy catalysts were similar to those over Cu and Ni metals, respectively.This result suggests that a hydrogen pretreatment of Cu-rich alloys forms a specific surface structure which is destroyed by evacuation at elevated temperatures.

Reactions of FeCH2(+) and CoCH2(+) with Aliphatic Alkanes in the Gas Phase. Activation of C-H and C-C Bonds by Naked Transition-Metal Carbene Ions

Jacobson, D. B.,Freiser, B. S.

, p. 4373 - 4378 (2007/10/02)

Gas-phase reactions of the title carbenes with several aliphatic alkanes using Fourier transform mass spectrometry (FTMS) ,are described.CoCH2(+) reacts with alkanes larger than methane whereas FeCH2(+) reacts with alkanes larger than ethane.Both FeCH2(+) and CoCH2(+) react predominantly by initial C-H bond insertion with some C-C bond insertion also observed.As a consequence of facile carbene-alkyl coupling, C-C bond cleavage processes proceed predominantly with elimination of the original carbene incorporated into the departing alkane neutral.In addition a small amount of C-C bond formation product is also observed.Finally, a greater degree of H/D scrambling is observed for CoCD2(+) than for FeCD2(+).

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