106869-53-8 Usage
Description
4-(6-Hydroxyhexyloxy)-4'-Methoxybiphenyl is a biphenyl derivative, an aromatic hydrocarbon consisting of two benzene rings connected by a carbon-carbon bond. 4-(6-HYDROXYHEXYLOXY)-4'-METHOXYBIPHENYL is distinguished by the presence of a hydroxyhexyloxy group on one benzene ring and a methoxy group on the other, endowing it with unique properties that make it valuable in various applications.
Uses
Used in Display Technologies:
4-(6-Hydroxyhexyloxy)-4'-Methoxybiphenyl is used as a liquid crystal material for the production of liquid crystal displays (LCDs) and other electronic devices. Its liquid crystal properties, such as low viscosity, high birefringence, and compatibility with other liquid crystal components, make it an ideal candidate for enhancing the performance of display technologies.
Used in Organic Electronics:
In the field of organic electronics, 4-(6-Hydroxyhexyloxy)-4'-Methoxybiphenyl is utilized for its potential to contribute to the development of advanced electronic components and devices. Its specific molecular structure allows for the exploration of its use in creating more efficient and versatile organic electronic materials.
Used in Photovoltaics:
4-(6-Hydroxyhexyloxy)-4'-Methoxybiphenyl may also find applications in the photovoltaic industry, where its properties could be harnessed to improve the performance of solar cells and other related technologies. Its potential use in this field is due to its ability to interact with light and its compatibility with other materials used in solar energy conversion processes.
Check Digit Verification of cas no
The CAS Registry Mumber 106869-53-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,8,6 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 106869-53:
(8*1)+(7*0)+(6*6)+(5*8)+(4*6)+(3*9)+(2*5)+(1*3)=148
148 % 10 = 8
So 106869-53-8 is a valid CAS Registry Number.
106869-53-8Relevant articles and documents
Identifying Structural Determinants of Mesomorphism from Focused Libraries of Tripedal Mesogens Prepared via the Passerini Three-Component Reaction
Song, Shuang,Sahoo, Dipankar,Kumar, Manoj,Barkley, Deborah A.,Heiney, Paul A.,Rudick, Jonathan G.
, p. 1195 - 1207 (2019)
Heterolithic tripedal mesogens are branched, multifunctional molecules that exhibit liquid crystalline properties. The liquid crystalline phase behavior of heterolithic tripedal mesogens can be challenging to predict from the structures of the different branches. To elucidate the structural basis for smectic mesomorphism in the first examples of heterolithic ABC tripedal mesogens, we synthesized and characterized six homolithic, three heterolithic AB2, and seven heterolithic ABC tripedes. The synthesis strategy took advantage of the Passerini three-component reaction to elaborate focused compound libraries in a combinatorial and high throughput manner. The phase behavior of the tripedes was characterized by a combination of polarized optical microscopy (POM), differential scanning calorimetry (DSC), and powder X-ray diffraction techniques. We show that one end-group of the heterolithic mesogens is responsible for the emergence of smectic mesomorphism in the presence of other groups that prefer nematic mesomorphism. Understanding how these structurally complex, non-conventional mesogens self-organize in liquid crystalline mesophases is significant for designing functional materials with predictable hierarchical order.
