14723-61-6 Usage
Uses
Used in Dye and Pigment Synthesis:
2,4-dinitro-1-(phenylsulfanyl)naphthalene is used as a chemical intermediate in the synthesis of dyes and pigments for various industrial applications. Its unique chemical structure contributes to the color and stability of the resulting dyes and pigments.
Used in Pesticide and Herbicide Formulations:
In the agricultural industry, 2,4-dinitro-1-(phenylsulfanyl)naphthalene is used as an active ingredient in pesticide and herbicide formulations. It is particularly effective in controlling broadleaf weeds, helping to protect crops and maintain healthy growth.
However, it is important to note that 2,4-dinitro-1-(phenylsulfanyl)naphthalene is considered potentially hazardous to human health and the environment. Therefore, it should be handled with care and in accordance with safety guidelines to minimize any adverse effects.
Check Digit Verification of cas no
The CAS Registry Mumber 14723-61-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,7,2 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 14723-61:
(7*1)+(6*4)+(5*7)+(4*2)+(3*3)+(2*6)+(1*1)=96
96 % 10 = 6
So 14723-61-6 is a valid CAS Registry Number.
14723-61-6Relevant academic research and scientific papers
Kinetic Studies of the Reactions of Some Phenyl Aryl Sulfides with Aliphatic Amines in Dimethyl Sulfoxide: the Mechanism of Base Catalysis
Chamberlin, Rachel A.,Crampton, Michael R.
, p. 425 - 432 (2007/10/02)
The reaction of n-butylamine, pyrrolidine and piperidine with 4'-R-phenyl 2,4,6-trinitrophenyl sulfides (R = H, Me, Br, NO2), 4a-d, result in the rapid formation of ?-adducts by attack at the unsubstituted 3-position; rate and equilibrium data are reported and substituent effects examined. Attack by amine at the 1-position of of 4a-d, phenyl 2,4-dinitronaphthyl sulfide 9, and phenyl 2,6-dinitro-4-trifluoromethyl sulfide 11, results in displacement of the phenylthio group.The substitutions by butylamine show a first order dependence on the amine concentration indicating that nucleophilic attack is rate determining.However the substitutions by pyrrolidine are subject to general base catalysis and it is argued that here the rate limiting step is deprotonation of the initially formed zwitterionic intermediate.
