152814-26-1 Usage
Uses
Used in Organic Synthesis:
3-Bromo-N-methylaniline, HCl is used as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for versatile chemical reactions, making it a valuable building block in the creation of new molecules with specific properties.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 3-Bromo-N-methylaniline, HCl is employed as a starting material for the development of new drugs. Its chemical properties enable the design and synthesis of potential therapeutic agents, contributing to the advancement of medicinal chemistry.
Used in Dye Manufacturing:
3-Bromo-N-methylaniline, HCl is utilized as a precursor in the production of dyes. Its chemical structure allows for the creation of dyes with specific color characteristics, making it an essential component in the dye manufacturing process.
Used in Industrial Chemical Production:
3-Bromo-N-methylaniline, HCl is also used in the synthesis of various industrial chemicals, where its unique properties can be leveraged to create products with specific applications in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 152814-26-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,8,1 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 152814-26:
(8*1)+(7*5)+(6*2)+(5*8)+(4*1)+(3*4)+(2*2)+(1*6)=121
121 % 10 = 1
So 152814-26-1 is a valid CAS Registry Number.
152814-26-1Relevant articles and documents
CROSSED EFFECT OF THE POLAR CHARACTERISTICS OF THE MEDIUM AND THE STRUCTURE OF THE SUBSTRATE IN THE REACTIONS OF AROYL CHLORIDES WITH N-METHYLANILINES
Shpan'ko, I. V.,Litvinenko, L. M.,Goncharov, A. N.,Korzhilova, O. I.
, p. 847 - 853 (2007/10/02)
A kinetic investigation was undertaken into the reactions of aroyl chlorides with 3-bromo- and 3-nitro-N-methylanilines in chlorobenzene, nitrobenzene, cyclohexane, and binary mixtures of chlorobenzene with nitrobenzene and cyclohexane at 25 deg C.The second-order rate constants of the reaction involving N-methyl-3-bromoaniline were treated by means of the Kirkwood, Hammet, and crossed structure-medium correlation equations.It was found that the correlations according to the Kirkwood and Hammet equation can be linear or broken, depending on the structure of the reagents and the characteristics of the medium.The presence of bends on the correlation curves is due to the appearance on the reaction coordinate in low-polarity media of a cyclic transition state, the formation of which is promoted by increase in the electron-withdrawing characteristics of the substituents in the benzene ring of both the amine and the aroyl chloride.The attainment of an isoparametric point with respect to the structure of the substrate in the region corresponding to the realization of the cyclic transition state was demonstrated by crossed correlation.
