50638-51-2 Usage
Description
4-Bromo-2-chloro-N,N-dimethylaniline, with the molecular formula C8H10BrClN, is a chemical compound derived from aniline. It features a bromine and chlorine substitution on the 4th and 2nd positions, respectively, and two methyl groups attached to the amine nitrogen. 4-BROMO-2-CHLORO-N,N-DIMETHYLANILINE is recognized for its role as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and dyes, as well as its utility as a reagent in organic synthesis and a precursor for other significant chemical compounds. Due to its toxic and harmful nature, it must be handled with caution in a controlled laboratory setting.
Uses
Used in Pharmaceutical Industry:
4-BROMO-2-CHLORO-N,N-DIMETHYLANILINE serves as a crucial intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with specific therapeutic properties, contributing to the advancement of medicine and healthcare.
Used in Agrochemical Industry:
In the agrochemical sector, 4-BROMO-2-CHLORO-N,N-DIMETHYLANILINE is utilized as an intermediate for the production of agrochemicals. Its involvement in the synthesis of these compounds helps address challenges in agriculture, such as pest control and crop protection, thereby supporting food security and sustainable farming practices.
Used in Dye Industry:
4-BROMO-2-CHLORO-N,N-DIMETHYLANILINE is also employed as an intermediate in the dye industry. Its chemical properties make it suitable for the creation of dyes with specific color characteristics and stability, which are essential for various applications, including textiles, plastics, and printing inks.
Used in Organic Synthesis:
As a reagent in organic synthesis, 4-BROMO-2-CHLORO-N,N-DIMETHYLANILINE plays a vital role in the preparation of other important chemical compounds. Its versatility in chemical reactions enables the synthesis of a wide range of products, further expanding the scope of its applications across different industries.
Used in Production of Other Chemical Compounds:
4-BROMO-2-CHLORO-N,N-DIMETHYLANILINE acts as a precursor for the production of other significant chemical compounds. Its involvement in the synthesis process is essential for creating new materials with unique properties, which can be applied in various fields, such as materials science, chemical research, and industrial processes.
Check Digit Verification of cas no
The CAS Registry Mumber 50638-51-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,6,3 and 8 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 50638-51:
(7*5)+(6*0)+(5*6)+(4*3)+(3*8)+(2*5)+(1*1)=112
112 % 10 = 2
So 50638-51-2 is a valid CAS Registry Number.
50638-51-2Relevant articles and documents
In situ Generation of Hypervalent Iodine Reagents for the Electrophilic Chlorination of Arenes
Granados, Albert,Jia, Zhiyu,del Olmo, Marc,Vallribera, Adelina
, p. 2812 - 2818 (2019/04/08)
Efficient metal-free methods for the electrophilic chlorination of arenes using PIFA and simple chlorine sources are reported. The in situ formation of PhI(Cl)OCOCF3 from PIFA and KCl is proposed, which resulted in a chlorinating species for moderately activated arenes. Moreover, the in situ formation of PhICl2 from PIFA and TMSCl resulted in an excellent approach for the chlorination of a great variety of arenes (20 examples) in high yields, even when working on a multigram scale.
The Chlorination of Some N,N-Dimethylanilines with 1,3,5-Trichloro-1,3,5-triazine-2,4,6-(1H,3H,5H)-trione (Trichloroisocyanuric Acid)
Rosevear, Judi,Wilshire, John F. K.
, p. 843 - 852 (2007/10/02)
The reaction of some representative N,N-dimethylanilines and of Fischer's base (1,3,3-trimethyl-2-methyleneindoline) with trichloroisocyanuric acid in concetrated sulfuric acid has been investigated.In many cases mixtures of chlorinated products were obtained; these mixtures were examined both by gas-liquid chromatography and by proton magnetic resonance spectroscopy.The reaction of N,N-dimethylaniline with dichloroisocyanuric acid was also studied.A feature of these chlorinations is the marked tendency for substitution to occur ortho to the dimethylamino group.This behaviour therefore differs from that reported for the corresponding brominations involving dibromoisocyanuric acid, where meta-substitution was observed.
