41825-73-4 Usage
Description
2-BROMO-4,6-DIMETHYLANILINE is an organic compound characterized by its white solid appearance. It is a derivative of aniline, with a bromine atom at the 2nd position and two methyl groups at the 4th and 6th positions. 2-BROMO-4,6-DIMETHYLANILINE is known for its reactivity in chemical processes, particularly in the synthesis of various organic compounds.
Uses
Used in Chemical Synthesis:
2-BROMO-4,6-DIMETHYLANILINE is used as a chemical intermediate for the production of other organic compounds. Its unique structure allows it to participate in various chemical reactions, leading to the formation of a wide range of products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-BROMO-4,6-DIMETHYLANILINE is used as a building block for the synthesis of various pharmaceutical compounds. Its reactivity and structural features make it a valuable component in the development of new drugs and medications.
Used in Dye and Pigment Industry:
2-BROMO-4,6-DIMETHYLANILINE is used as a starting material for the synthesis of dyes and pigments. Its chemical properties enable it to be transformed into a variety of colored compounds, which can be used in various applications such as textiles, plastics, and printing inks.
Used in Research and Development:
In the field of research and development, 2-BROMO-4,6-DIMETHYLANILINE serves as a valuable compound for studying various chemical reactions and mechanisms. Its unique structure and reactivity make it an interesting subject for scientific investigations, potentially leading to new discoveries and advancements in the field of chemistry.
For example, the reaction of 2-BROMO-4,6-DIMETHYLANILINE with 3-chloro-3-methyl-but-1-yne to produce 2-bromo-N-(1',1'-dimethylprop-2'-ynyl)-4,6-dimethylaniline requires the use of reagent Et3N, catalyst CuCl, and the menstruum dioxane. This reaction demonstrates the compound's utility in chemical synthesis and its potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 41825-73-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,8,2 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 41825-73:
(7*4)+(6*1)+(5*8)+(4*2)+(3*5)+(2*7)+(1*3)=114
114 % 10 = 4
So 41825-73-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H10BrN/c1-5-3-6(2)8(10)7(9)4-5/h3-4H,10H2,1-2H3
41825-73-4Relevant articles and documents
Nitromethane as a reagent for the synthesis of 3-nitroindoles from 2-haloarylamine derivatives
Chesnokov,Ageshina,Maryanova,Rzhevskiy,Gribanov,Topchiy,Nechaev,Asachenko
, p. 2370 - 2377 (2020/12/31)
A new approach to the synthesis of 3-nitroindoles using palladium-catalyzed arylation of nitromethane with N-(2-bromoaryl)imidates was developed. A convenient and rapid method for cyclization of ethyl N-(2-nitromethylaryl)acetimidates to 2-methyl-3-nitro-1H-indoles was proposed.
Direct Synthesis of Structurally Divergent Indole Alkaloids from Simple Chemicals
Shen, Tao,Zhu, Bencong,Lin, Fengguirong,Pan, Jun,Wei, Jialiang,Luo, Xiao,Liu, Jianzhong,Jiao, Ning
supporting information, p. 815 - 818 (2018/07/31)
A direct and structurally divergent synthesis of indole alkaloids from very simple 2-vinylanilines, alkynes and TBN via a novel substrate fragmentation/cycloaddition strategy has been developed, which provides an efficient noble-metal-free approach to access a library of highly valuable indole derivatives of tryptamines and tryptamine-related oximes, lactams, and lactones, as well as β-carbolines, spiroindolines, and hexa-hydropyrrolo[2,3-b]indoles.
