128259-71-2 Usage
Uses
Used in Chemical Synthesis Industry:
2,5-DIBROMO-1,3-DIFLUOROBENZENE is used as a key intermediate in the synthesis of advanced organic compounds. Its unique structure allows for targeted functionalization and the formation of new chemical bonds, which is crucial for creating complex molecules with specific properties.
Used in Liquid Crystal Compounds Production:
2,5-DIBROMO-1,3-DIFLUOROBENZENE is used as a starting material for the preparation of bicyclohexylylacetylene and bicyclohexyl-containing diyne liquid crystal compounds. These liquid crystal compounds are essential in the development of display technologies, such as liquid crystal displays (LCDs), due to their ability to manipulate light and respond to electric fields.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, the unique structure and properties of 2,5-DIBROMO-1,3-DIFLUOROBENZENE may also make it a potential candidate for the development of new pharmaceutical agents. Its halogenated aromatic nature could be exploited in the design of novel drug molecules with specific biological activities, potentially leading to the discovery of new treatments for various diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 128259-71-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,2,5 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 128259-71:
(8*1)+(7*2)+(6*8)+(5*2)+(4*5)+(3*9)+(2*7)+(1*1)=142
142 % 10 = 2
So 128259-71-2 is a valid CAS Registry Number.
128259-71-2Relevant academic research and scientific papers
PHOTOCHEMICAL BROMINATION OF ARENES. 2. FLUOROBENZENE DERIVATIVES (1)
Bolton, Roger,Owen, Elaine S. E.
, p. 393 - 406 (2007/10/02)
Photochemically induced reaction of fluorobenzene and a range of polyfluorobenzenes, both in an excess of the arene and with fluorotrichloromethane as solvent, gave isolable adducts only with fluorobenzene, the isomeric difluorobenzenes, and in very small yield with 1,3,5-trifluorobenzene.These adducts were identified by combustion analysis, mass spectrometry, and n.m.r. techniques (1H, 13C, 19F).In every case, the expected substitution products accompanied these adducts, and in the more fully fluorinated benzene derivatives substitution was the only process observed.Fluorotrichloromethane encouraged the formation of adducts, but the concurrent formation of substantial amounts of substitution products suggested that adducts are not the necessary precursors of the substitution products, in contrast with other systems.
