28864-96-2 Usage
Description
Biphenyl, 4-(4-methylcyclohexyl)-, transis a chemical compound characterized by the molecular formula C19H20. It represents a trans isomer of 4-(4-methylcyclohexyl)biphenyl, where the two aromatic rings are positioned in a trans configuration. Biphenyl, 4-(4-methylcyclohexyl)-, transis distinguished by its role in the creation of liquid crystals, which are integral to numerous electronic applications.
Uses
Used in Electronics Industry:
Biphenyl, 4-(4-methylcyclohexyl)-, transis utilized as a key component in the production of liquid crystals, which are vital for the functioning of flat panel displays and solar cells. Biphenyl, 4-(4-methylcyclohexyl)-, trans-'s structural properties make it suitable for these applications, contributing to the advancement of electronic devices.
Used in Chemical Synthesis:
Biphenyl, 4-(4-methylcyclohexyl)-, transalso serves as a raw material in the synthesis of various organic compounds. Its unique structure allows it to be a valuable intermediate in chemical reactions, facilitating the creation of a range of products in the chemical industry.
Used in Industrial and Research Settings:
Recognized for its low toxicity, Biphenyl, 4-(4-methylcyclohexyl)-, transis considered relatively safe for handling in both industrial and research environments. This safety profile is advantageous for workers and researchers, reducing potential health risks associated with chemical exposure.
Check Digit Verification of cas no
The CAS Registry Mumber 28864-96-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,8,6 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 28864-96:
(7*2)+(6*8)+(5*8)+(4*6)+(3*4)+(2*9)+(1*6)=162
162 % 10 = 2
So 28864-96-2 is a valid CAS Registry Number.
InChI:InChI=1/C19H22/c1-15-7-9-17(10-8-15)19-13-11-18(12-14-19)16-5-3-2-4-6-16/h2-6,11-15,17H,7-10H2,1H3/t15-,17-
28864-96-2Relevant articles and documents
Efficient cross-coupling of secondary alkyltrifluoroborates with aryl chlorides-reaction discovery using parallel microscale experimentation
Dreher, Spencer D.,Dormer, Peter G.,Sandrock, Deidre L.,Molander, Gary A.
supporting information; body text, p. 9257 - 9259 (2009/02/02)
Microscale parallel experimentation was used to discover three catalyst systems capable of coupling secondary organotrifluoroborates with sterically and electronically demanding aryl chlorides and bromides. The ensuing results represent the first comprehensive study of alkylboron coupling to aryl chlorides and, in particular, using secondary alkylboron partners. A ligand-dependent β-hydride elimination/reinsertion mechanism was implicated in the cross-coupling of more hindered substrates, leading to isomeric mixtures of coupled products in some cases. Copyright
