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1,3,5-trifluoro(2,4,6-d3)benzene is a deuterated analog of 1,3,5-trifluorobenzene, a halogenated aromatic. compound It consists of a benzene ring with three fluorine atoms at the 1, 3, and 5 positions and three deuterium atoms at the 2, 4, and 6 positions. 1,3,5-trifluoro(2,4,6-d3)benzene is often used as a reference material in nuclear magnetic resonance (NMR) spectroscopy due to its unique chemical structure and deuterium labeling, which allows for accurate determination of chemical shifts and improved signal resolution. Its applications span across various fields, including chemical research, pharmaceutical development, and materials science, where it serves as a valuable tool for studying molecular interactions and structural properties.

1423-08-1

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1423-08-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1423-08-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,2 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1423-08:
(6*1)+(5*4)+(4*2)+(3*3)+(2*0)+(1*8)=51
51 % 10 = 1
So 1423-08-1 is a valid CAS Registry Number.

1423-08-1Upstream product

1423-08-1Downstream Products

1423-08-1Relevant academic research and scientific papers

Thermoneutral Isotope Exchange Reactions of Cations in the Gas Phase

Ausloos, P.,Lias, S. G.

, p. 3641 - 3647 (1981)

Rate constants have been measured for reactions of the type AD2+ + MH --> MD + ADH+, where AD2+ is CD3CND+, CD3CDOD+, (CD3COCD3)D+, or (C2D5)2OD+ and the MH molecules are alcohols, acids, mercaptanes, H2S, AsH3, PH3, or aromatic molecules.Rate constants are also presented for the reactions ArHD+ + D2O --> ArDD+ + HDO, where ArHD+ is a deuteronated aromatic molecule and ArDD+ is the same species with a D atom incorporated on the ring.In all but two cases, the competing deuteron transfer is sufficiently endothermic that it cannot be observed under the conditions of the ICR experiments at 320 - 420 K.The efficiencies of the isotope exchange reactions are interpreted in terms of estimated potential surface cross sections for the reactions AD2+ + MH --> 2+*MH> --> +> --> +*MD> --> ADH+ + MD.When the formation of the +> complex is estimated to be thermoneutral or slightly endothermic, the isotope exchange process is inefficient (probability of a reactive collision 2+*MH> --> +> is exothermic.For most of the systems, trends in reaction efficiency appear to be related to factors such as dipole moments of reactant species (or for aromatic compounds, the electron-donating or -withdrawing properties of ring substituents) which influence the relative orientation of the two reactant species in the complex.

Deuterium Exchange between Arenes and Deuterated Solvents in the Absence of a Transition Metal: Synthesis of D-Labeled Fluoroarenes

Salamanca, Vanesa,Albéniz, Ana C.

supporting information, p. 3206 - 3212 (2020/04/15)

Fluoroarenes can be selectively deuterated by H/D exchange with common deuterated solvents in the presence of a catalytic amount of an alkali metal carbonate or, for the less acidic arenes, stoichiometric quantities of potassium phosphate. This is a susta

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