1802566-49-9 Usage
Uses
Used in Pharmaceutical Industry:
ALPHA,ALPHA'-IMINODI-P-TOLUNITRILE HYDROCHLORIDE is used as a starting material for the synthesis of various pharmaceutical products due to its ability to form a wide range of biologically active compounds.
Used in Agricultural Industry:
ALPHA,ALPHA'-IMINODI-P-TOLUNITRILE HYDROCHLORIDE is used as a starting material for the synthesis of various agricultural products, contributing to the development of effective and safe agrochemicals.
Used in Fine Chemicals Production:
ALPHA,ALPHA'-IMINODI-P-TOLUNITRILE HYDROCHLORIDE is used as a versatile intermediate in the production of fine chemicals, enabling the creation of a diverse array of chemical compounds.
Used in Dyes Synthesis:
ALPHA,ALPHA'-IMINODI-P-TOLUNITRILE HYDROCHLORIDE is used as a key building block in the synthesis of dyes, contributing to the development of new and improved colorants for various applications.
Used in Heterocycles Synthesis:
ALPHA,ALPHA'-IMINODI-P-TOLUNITRILE HYDROCHLORIDE is used as a reagent in the synthesis of heterocycles, which are important in the development of pharmaceuticals, agrochemicals, and other specialty chemicals.
It is important to handle ALPHA,ALPHA'-IMINODI-P-TOLUNITRILE HYDROCHLORIDE with care due to its potential hazards, and it should be used in a controlled laboratory setting with appropriate safety measures in place.
Check Digit Verification of cas no
The CAS Registry Mumber 1802566-49-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,8,0,2,5,6 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1802566-49:
(9*1)+(8*8)+(7*0)+(6*2)+(5*5)+(4*6)+(3*6)+(2*4)+(1*9)=169
169 % 10 = 9
So 1802566-49-9 is a valid CAS Registry Number.
1802566-49-9Relevant academic research and scientific papers
Computationally forecasting the effect of dibenzylammonium substituents on pseudorotaxane formation with dibenzo[24]crown-8
Payne, Nicholas A.,Delmas, Luke C.,McDowell, Sean A.C.,Williams, Avril R.
supporting information, p. 5175 - 5179 (2015/08/18)
The ability to predict the relative stabilities of analogous pseudorotaxanes is essential for the synthetic chemist yet simplified computational forecasting approaches remain scarce. Consequently, ten [2]pseudorotaxanes have been assembled (from a series of para-substituted dibenzylammonium ions and dibenzo[24]crown-8) and their experimentally-determined stabilities correlated with two computational parameters closely related to complexation energy. The strongest relationship was obtained from density functional theory calculation of binding energy (R2 = 0.92) while determination of the maximum surface electrostatic potential on the dibenzylammonium ions (a proxy indicator of complex stability) afforded comparable results (R2 = 0.88) with great reduction in computational expense.
