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α-Sodiophenylacetonitrile, also known as sodium phenylacetonitrile, is an organic compound with the chemical formula C8H6NaNS. It is a white crystalline solid that is soluble in water and polar organic solvents. α-sodiophenylacetonitrile is formed by the deprotonation of phenylacetonitrile, where a sodium atom replaces the hydrogen atom on the α-carbon. α-Sodiophenylacetonitrile is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds due to its reactivity and versatility. It can participate in various chemical reactions, such as nucleophilic substitution, addition, and elimination reactions, making it a valuable building block in organic synthesis.

14904-38-2

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14904-38-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14904-38-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,9,0 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 14904-38:
(7*1)+(6*4)+(5*9)+(4*0)+(3*4)+(2*3)+(1*8)=102
102 % 10 = 2
So 14904-38-2 is a valid CAS Registry Number.

14904-38-2Upstream product

14904-38-2Relevant academic research and scientific papers

Carboanion Reactivity: Kinetics of the Reactions of Benzyl Cyanide Anions with Aromatic Nitro-compounds

Atherton, John H.,Crampton, Michael R.,Duffield, Gaynor L.,Stevens, J. Andrew

, p. 443 - 448 (1995)

Rate and equilibrium measurements are reported for the reactions in methanol of carbanions derived from 12 ring-substituted benzyl cyanides with 1,3,5-trinitrobenzene to give ?-adducts.Some data for reaction of the carbanions with 4-nitrobenzofuroxan were also measured.With increasing carbanion reactivity, rate constants approach a limit of just below 109 dm3 mol-1 s-1.Intrinsic reactivities of carbanions in ?-adduct forming reactions and in proton transfer reactions are compared.

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