117692-99-6 Usage
Uses
Used in Organic Synthesis:
4-Benzyloxy-4'-bromo-biphenyl is used as a building block for the synthesis of biologically active molecules, leveraging its structural features to create a variety of compounds with potential therapeutic or functional properties.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 4-Benzyloxy-4'-bromo-biphenyl is employed as a key intermediate in the development of pharmaceuticals, contributing to the discovery of new drugs and therapeutic agents.
Used in Coordination Chemistry:
4-Benzyloxy-4'-bromo-biphenyl serves as a ligand in coordination chemistry, playing a crucial role in the formation and stabilization of metal complexes, which can have applications in catalysis, sensing, and other areas.
Used in Pharmaceutical Development:
4-Benzyloxy-4'-bromo-biphenyl is utilized in the pharmaceutical industry as a starting material for the preparation of derivatives with potential applications in drug discovery and development, aiming to address unmet medical needs.
Used in Agrochemical Research:
In agrochemicals, 4-Benzyloxy-4'-bromo-biphenyl is used to develop new compounds for pest control and crop protection, capitalizing on its chemical properties to enhance the effectiveness of agrochemical products.
Used in Material Science:
4-Benzyloxy-4'-bromo-biphenyl contributes to material science by being a component in the synthesis of new materials with specific properties, such as conductivity, stability, or responsiveness to environmental stimuli.
Used in Academic Research:
In academic research, 4-Benzyloxy-4'-bromo-biphenyl is used to study structure-activity relationships, providing insights into how molecular structure influences biological activity and guiding the design of more effective compounds.
Used in the Development of Synthetic Methodologies:
4-Benzyloxy-4'-bromo-biphenyl is instrumental in the development of new synthetic methodologies, facilitating the advancement of chemical synthesis techniques and enabling the production of complex molecules more efficiently and selectively.
Check Digit Verification of cas no
The CAS Registry Mumber 117692-99-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,6,9 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 117692-99:
(8*1)+(7*1)+(6*7)+(5*6)+(4*9)+(3*2)+(2*9)+(1*9)=156
156 % 10 = 6
So 117692-99-6 is a valid CAS Registry Number.
117692-99-6Relevant academic research and scientific papers
Self-assembling molecular dumbbells: From nanohelices to nanocapsules triggered by guest intercalation
Ryu, Ja-Hyoung,Kim, Ho-Joong,Huang, Zhegang,Lee, Eunji,Lee, Myongsoo
, p. 5304 - 5307 (2007/10/03)
(Figure Presented) Dumbbells that are not dumb: Dumbbell-shaped molecules based on a hexa-p-phenylene derivative self-assemble into well-defined left-handed helical fibers in aqueous solution. These helical nanofibers convert reversibly into hollow nanocapsules by intercalation of aromatic guest molecules (red spheres).
Polymerizable compound, polymerizable resin composition, cured polymer and liquid crystal display device
-
Page column 41, (2010/02/05)
The polymerizable compound of this invention is represented by general formula (I): where R is H, R′, R′O, R′COO, or R′OCO, R′ is a linear or branched alkyl group or alkenyl group having 1 to about 15 carbon atoms, A1 and A2 are independently a cyclohexane ring or a benzene ring which may include a substituent represented by formula (II) below; X is H or CH3; and Y1, Y2, Y3, and Y4 are independently H, F, Cl, CH3, CH3O, CF3, or CF3O wherein at least two of Y1, Y2, Y3, and Y4 are H and, if both A1 and A2 are cyclohexane rings, at least one of Y1, Y2, Y3, and Y4 is not H: where Y5, Y6, Y7, and Y8 are independently H, F, Cl, CH3, CH3O, CF3, or CF3O, at least two of Y5, Y6, Y7, and Y8 are H.
