24932-48-7 Usage
Description
4,5-DIBROMO-O-XYLENE is an organic compound with the chemical formula C8H8Br2. It is a white solid that can be synthesized through the bromination of o-xylene. 4,5-DIBROMO-O-XYLENE is known for its various applications across different industries, particularly in the synthesis of various chemicals and pharmaceuticals.
Uses
Used in Pharmaceutical Industry:
4,5-DIBROMO-O-XYLENE is used as a reagent for the synthesis of Thalidomide (T338850), which is an inhibitor of FGF-induced angiogenesis and replication of human immunodeficiency virus type 1. Thalidomide is also a teratogenic sedative and immunomodulatory agent, primarily used in combination with dexamethasone to treat multiple myeloma.
Used in Photodynamic Therapy:
In the field of photodynamic therapy, 4,5-DIBROMO-O-XYLENE can be utilized in the synthesis of alkylamino zinc(II)phthalocyanines. These compounds have potential applications as photosensitizers, which are crucial components in the treatment process of photodynamic therapy.
Used in Chemical Synthesis:
4,5-DIBROMO-O-XYLENE is also used in the synthesis of 1,2-dibromo-4,5-bis(dibromomethyl)benzene through a reaction with azobisisobutyronitrile. This synthesized compound can have further applications in various chemical processes and industries.
Check Digit Verification of cas no
The CAS Registry Mumber 24932-48-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,9,3 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 24932-48:
(7*2)+(6*4)+(5*9)+(4*3)+(3*2)+(2*4)+(1*8)=117
117 % 10 = 7
So 24932-48-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H8Br2/c1-5-3-7(9)8(10)4-6(5)2/h3-4H,1-2H3
24932-48-7Relevant articles and documents
Peripherally octamethyl zinc(II) phthalocyanines with various axial substituents
Janczak, Jan
, (2021)
A series of zinc(II) phthalocyanine complexes peripherally octa-substituted by methyl groups and with axially ligated N-donor ligands, (Zn(Me)8Pc-L, where L is pyridine (4), 3-methylpyridine (5), 3,4-lutidine (6) and 3,5-lutidine (7)), was synt
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Naidis et al.
, (1974)
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Multisubstituted C2-symmetric ansa -metallocenes bearing nitrogen heterocycles: Influence of substituents on catalytic properties in propylene polymerization at higher temperatures
Canich, Jo Ann M.,Goryunov, Georgy P.,Izmer, Vyatcheslav V.,Kononovich, Dmitry S.,Kulyabin, Pavel S.,Sharikov, Mikhail I.,Uborsky, Dmitry V.,Voskoboynikov, Alexander Z.
supporting information, p. 6170 - 6180 (2021/05/19)
In this work we systematically studied the effects of modifications of substituents on the performance of the isospecific zirconocene-based catalyst family, Me2Si(2-Alk-4-(N-carbazolyl)Ind)ZrX2 (X = Cl, Me), wherein the progenitor was shown to be particul
Subnaphthalocyanine triimides: Potential three-dimensional solution processable acceptors for organic solar cells
Cai, Chunsheng,Chen, Shanshan,Li, Li,Yuan, Zhongyi,Zhao, Xiaohong,Zhang, Youdi,Hu, Yu,Yang, Changduk,Hu, Ming,Huang, Xiaoshuai,Chen, Xuanwen,Chen, Yiwang
, p. 2186 - 2195 (2020/02/22)
Subnaphthalocyanine triimides (SubNcTIs) as solution processable electron acceptors were designed and synthesized by introducing three electron-withdrawing imide groups to subnaphthalocyanines. Their solubility and crystallinity could be adjusted convenie