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4-cyano-N-benzylpyridinium chloride is a chemical compound with the molecular formula C13H11ClN2. It is a derivative of pyridinium, featuring a cyano group (-CN) at the 4-position and a benzyl group (C6H5-CH2-) attached to the nitrogen atom. This organic salt is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as a reagent in organic chemistry. The compound is typically obtained as a white crystalline solid and is soluble in organic solvents. Due to its reactivity, it is often used in the formation of various heterocyclic compounds and as a building block in the development of new chemical entities.

1966-86-5

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1966-86-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1966-86-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,6 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1966-86:
(6*1)+(5*9)+(4*6)+(3*6)+(2*8)+(1*6)=115
115 % 10 = 5
So 1966-86-5 is a valid CAS Registry Number.

1966-86-5Downstream Products

1966-86-5Relevant academic research and scientific papers

The Importance of Hydrophobic-Hydrophilic Factors in Binding of Charged Substrates to Micelles: The Use of Extramicellar Probe Luminescence to Monitor Association of Cations to the Micelle

Foreman, Thomas K.,Sobol, Warren M.,Whitten, David G.

, p. 5333 - 5336 (1981)

The anionic metal complexes 1, RuL34-, where L = 4,4'-dicarboxy-2,2'-bipyridine, has been used as an extramicellar lumeniscent probe to monitor the binding capacity of anionic sodium dodecylsulfate micelles for the quencher Cu2+ and several organic cations.Addition of surfactant attenuates the quenching activity of the cations toward 1 in each case.For Cu2+ the binding capacity, as monitored by the quenching of the extramicellar probe, is in good agreement with those determined for Cu2+ and other divalent metal ions, using quite different methods; curvature in the quenching plot as 2+> increases is attributed to screening of the micellar charge by bound Cu2+.For MV2+ quite different behavior is observed; the Stern-Volmer type quenching plot shows two good linear portions at any surfactant concentration.The portion with low slope at low 2+> is attributed to MV2+ binding to the organized surfactant; at higher 2+> the steeper plot has a slope essentially the same as that obtained in water in the absence of micelles.The absence of curvature suggests association of several MV2+ molecules does not inhibit binding of additional quenchers until nearly all the binding sites are occupied.This finding, combined with the relatively high binding capacity in terms of cation/SDS for MV2+ compared to metal ions, suggests that MV2+ binds at different sites and that other factors control its binding.Similar results heve been obtained with other organic cations.The results are most consistent with a model whereby these bind at hydrocarbon-water interfaces and not primarily with the micelle head groups.

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