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60291-29-4

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60291-29-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60291-29-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,2,9 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 60291-29:
(7*6)+(6*0)+(5*2)+(4*9)+(3*1)+(2*2)+(1*9)=104
104 % 10 = 4
So 60291-29-4 is a valid CAS Registry Number.

60291-29-4Downstream Products

60291-29-4Relevant academic research and scientific papers

Dynamics of the gas-phase reactions of chloride ion with fluoromethane: High excess translational activation energy for an endothermic SN2 reaction

Angel, Laurence A.,Garcia, Sandra P.,Ervin, Kent M.

, p. 336 - 345 (2007/10/03)

Guided ion beam tandem mass spectrometry techniques are used to examine the competing product channels in the reaction of Cl- with CH3F in the center-of-mass collision energy range 0.05-27 eV. Four anionic reaction products are detected: F-, CH2Cl-, FCl- and CHCl-. The endothermic SN2 reaction Cl- + CH3F → CH3Cl + F- has an energy threshold of E0 = 181 ± 14 kJ/mol, exhibiting a 52 ± 16 kJ/mol effective barrier in excess of the reaction endothermicity. The potential energy of the SN2 transition state is well below the energy of the products. Dynamical impedances to the activation of the SN2 reaction are discussed, including angular momentum constraints, orientational effects, and the inefficiency of translational energy in promoting the reaction. The fluorine abstraction reaction to form CH3 + FCl- exhibits a 146 ± 33 kJ/mol effective barrier above the reaction endothermicity. Direct proton transfer to form HCl is highly inefficient, but HF elimination is observed above 268 ± 95 kJ/mol. Potential energy surfaces for the reactions are calculated using the CCSD(T)/aug-cc-pVDZ and HF/6-31+G(d) methods and used to interpret the dynamics.

Gas-phase Acidity of CH3X Compounds

Ingemann, Steen,Nibbering, Nico M.M.

, p. 837 - 840 (2007/10/02)

Proton abstraction from (CH3)3P, CH3SCH3, CH3Cl, CH3Br, and CH3I in the gas phase has been investigated with the use of Fourier transform ion cyclotron resonance (FT - ICR) mass spectrometry.The gas-phase acidities of the three former compounds are reported to be ΔG0acid 1 606 +/- 8 kJ mol-1; ΔG0acid (CH3SCH3) 1 616 +/- 8 kJ mol-1; and ΔG0acid (CH3Cl) 1 628 +/- 12 kJ mol-1.The competition between proton abstraction and SN2 substitution in the reactions of different anions with CH3F, CH3Cl, CH3Br, and CH3I has been determined.Based upon these kinetic experiments, it is concluded that the gas-phase acidity increases down the series CH3F, CH3Cl, CH3Br, CH3I.The reactions of (CH3)2PCH2-, ClCH2-, and BrCH2- ions with various molecules are described.

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