220844-83-7 Usage
Uses
Used in Pharmaceutical Research and Development:
3-bromo-4-(dimethylamino)benzoic acid is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the creation of drugs targeting a wide array of diseases and conditions, making it a valuable asset in medicinal chemistry.
Used in Agrochemical Production:
In the agrochemical industry, 3-bromo-4-(dimethylamino)benzoic acid is utilized as a precursor for the development of crop protection agents. Its properties contribute to the formulation of effective pesticides and other agricultural chemicals that protect crops from pests and diseases.
Used in the Synthesis of Fluorescent Dyes:
3-bromo-4-(dimethylamino)benzoic acid is employed as a starting material in the production of fluorescent dyes. These dyes have applications in various fields, including bioimaging, diagnostics, and as markers in research settings, capitalizing on the compound's inherent fluorescent properties.
Used in Advanced Material Creation:
3-bromo-4-(dimethylamino)benzoic acid also serves as a precursor in the synthesis of advanced materials. Its role in material science is significant for developing new technologies and improving existing ones, such as in the creation of sensors, optoelectronic devices, and other high-tech applications where specific material properties are required.
Check Digit Verification of cas no
The CAS Registry Mumber 220844-83-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,8,4 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 220844-83:
(8*2)+(7*2)+(6*0)+(5*8)+(4*4)+(3*4)+(2*8)+(1*3)=117
117 % 10 = 7
So 220844-83-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H10BrNO2/c1-11(2)8-4-3-6(9(12)13)5-7(8)10/h3-5H,1-2H3,(H,12,13)
220844-83-7Relevant academic research and scientific papers
Catalyst and Additive-Free Direct Amidation/Halogenation of Tertiary Arylamines with N-haloimide/amides
Xu, Xiu-Juan,Amuti, Adila,Wusiman, Abudureheman
supporting information, p. 5002 - 5008 (2020/10/06)
An approach has been developed for the amidation (halogenation) of tertiary arylamines by electrophilic activation using N-haloimide/amides. Several control experiments have been performed, and the coupling reaction outcomes indicated that the N-haloimide/amide brings three major functions, including electrophilic activation, aromatic halogenation and nucleophilic nitrogen sources. This cascade reaction features simple manipulation, requires no additional catalyst, oxidant or additives, and is performed under mild conditions. (Figure presented.).
