7149-14-6 Usage
Uses
Used in Organic Synthesis:
2-Bromo-1-iodo-4-nitrobenzene is utilized as a building block in organic synthesis, particularly for the production of pharmaceuticals and agrochemicals. Its versatile nature allows it to serve as an intermediate in the synthesis of a variety of organic compounds, including dyes, pigments, and other fine chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Bromo-1-iodo-4-nitrobenzene is used as a key intermediate for the synthesis of various medicinal compounds. Its unique substitution pattern and reactivity make it a valuable component in the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
2-Bromo-1-iodo-4-nitrobenzene is also employed in the agrochemical industry as a precursor for the synthesis of various agrochemicals, such as pesticides and herbicides. Its ability to participate in different chemical reactions contributes to the creation of effective and targeted agrochemical products.
Used in Chemical Intermediates for Electronic Materials:
Furthermore, 2-Bromo-1-iodo-4-nitrobenzene is used in the production of chemical intermediates for the manufacture of electronic materials. Its involvement in the synthesis of these materials aids in the development of advanced electronic components and devices.
Used in Specialty Chemicals Production:
Additionally, 2-Bromo-1-iodo-4-nitrobenzene is utilized in the production of specialty chemicals, where its unique properties and reactivity contribute to the creation of high-value chemical products for various applications.
Used in Organic Chemistry as a Reagent:
2-Bromo-1-iodo-4-nitrobenzene is also used as a reagent in organic chemistry, participating in various reactions such as Suzuki-Miyaura cross-coupling and palladium-catalyzed cross-coupling. Its role in these reactions facilitates the synthesis of complex organic molecules and contributes to the advancement of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 7149-14-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,4 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7149-14:
(6*7)+(5*1)+(4*4)+(3*9)+(2*1)+(1*4)=96
96 % 10 = 6
So 7149-14-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H3BrINO2/c7-5-3-4(9(10)11)1-2-6(5)8/h1-3H
7149-14-6Relevant academic research and scientific papers
Rhodium-Catalyzed Synthesis and Optical Properties of Silicon-Bridged Arylpyridines
Shintani, Ryo,Misawa, Nana,Takano, Ryo,Nozaki, Kyoko
supporting information, p. 2660 - 2665 (2017/03/06)
A convergent and regioselective synthesis of silicon-bridged 4-arylpyridines has been developed through a rhodium-catalyzed [2+2+2] cycloaddition of silicon-containing diynes with nitriles. The absorption and emission properties of these compounds have be
IMIDAZOQUINOLINE COMPOUNDS AS BROMODOMAIN INHIBITORS
-
Page/Page column 102, (2015/04/22)
The present invention provides compound of formula (I), or an isotopic form, a stereoisomer, a tautomer, a pharmaceutically acceptable salt, a solvate, a polymorph, a prodrug, N-oxide or S-oxide thereof; and processes for their preparation. The invention further relates to pharmaceutical compositions containing said compounds and their use in the treatment of diseases or disorders mediated by bromodomain containing proteins, particularly cancer.
Tribromoisocyanuric acid in trifluoroacetic acid: An efficient system for smooth brominating of moderately deactivated arenes
De Almeida, Leonardo S.,De Mattos, Marcioc. S.,Esteves, Pierre M.
, p. 603 - 606 (2013/04/10)
Moderately deactivated arenes are efficiently brominated by the reaction with tribromoisocyanuric acid (0.34 mol equiv) in trifluoroacetic acid at room temperature in 48-85% isolated yield. This medium avoids the polybromination of the substrate, observed in the same reaction performed in 98% H 2SO4. Georg Thieme Verlag Stuttgart · New York.
