97730-31-9 Usage
Description
(S)-4'-(2-Methylbutyl)Biphenyl-4-Carbonitrile, also known as 4'-[(S)-2-Methylbutyl]-4-Biphenylcarbonitrile, is a chemical compound with the molecular formula C22H23N. It is a biphenyl derivative with a nitrile functional group attached to one of the benzene rings. (S)-4'-(2-Methylbutyl)Biphenyl-4-Carbonitrile is recognized for its potential applications in various fields, including organic synthesis, pharmaceutical research, and material science.
Uses
Used in Organic Synthesis:
(S)-4'-(2-Methylbutyl)Biphenyl-4-Carbonitrile is used as a building block in organic synthesis for the creation of more complex molecules. Its unique structure allows for versatile chemical reactions, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Research:
In pharmaceutical research, (S)-4'-(2-Methylbutyl)Biphenyl-4-Carbonitrile serves as a key intermediate in the development of new drugs. Its properties can be leveraged to design and synthesize novel therapeutic agents with potential applications in treating a variety of diseases and conditions.
Used in Liquid Crystal Displays:
(S)-4'-(2-Methylbutyl)Biphenyl-4-Carbonitrile has been studied for its potential applications in liquid crystal displays. Its molecular structure may contribute to the development of advanced materials with improved performance characteristics, such as enhanced stability and response times, which are crucial for the next generation of display technologies.
Used as a Fluorescent Probe:
(S)-4'-(2-Methylbutyl)Biphenyl-4-Carbonitrile has also been explored as a fluorescent probe in various analytical and diagnostic applications. Its optical properties can be utilized to detect and monitor chemical processes, biological interactions, or environmental contaminants, providing valuable insights into complex systems.
Used in Therapeutic Research:
(S)-4'-(2-Methylbutyl)Biphenyl-4-Carbonitrile has been the subject of research for its potential therapeutic properties. Its unique chemical structure may offer new avenues for the treatment of various diseases and conditions, making it a promising candidate for further investigation and development in the field of medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 97730-31-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,7,3 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 97730-31:
(7*9)+(6*7)+(5*7)+(4*3)+(3*0)+(2*3)+(1*1)=159
159 % 10 = 9
So 97730-31-9 is a valid CAS Registry Number.
97730-31-9Relevant articles and documents
An Efficient Asymmetric Synthesis of a Liquid Crystal
Tius, Marcus A.,Gu, Xue-qin,Truesdell, Joel W.,Savariar, Selvaraj,Crooker, P. P.
, p. 36 - 40 (2007/10/02)
A synthesis of L-(-)-4-(2-methylbutyl)phenyl4'-(2-methylbutyl)biphenyl-4-carboxylate (CE2) and of related chiral liquid crystals has been reported; nevertheless, a detailed experimental and spectrometric characterization of both the intermediates and the final product has been lacking in the literature.We present here the first synthesis of the enantiomer of CE2 with full experimental details including spectroscopic data for each of the intermediates.The description of the synthesis of (R)-(+)-2-methylbutanyl will be broadly useful for preparing other liquid crystals with optically active (R)-2-methylbutyl side chains.
MESOMORPHIC TRANSITION TEMPERATURES AND VISCOSITIES FOR SOME CYANO-BIPHENYLS AND -p-TERPHENYLS WITH BRANCHED TERMINAL ALKYL GROUPS.
Gray,Kelly
, p. 335 - 345 (2007/10/02)
A number of 4-alkyl- and 4-alkoxy-4 prime -cyanobiphenyls and 4-alkyl-4 double prime -cyano-p-terphenyls with branched chains were prepared. Marked depressions in the liquid crystal transition temperatures were observed relative to those for the corresponding n-alkyl derivatives, although the melting points were affected to a smaller extent. The viscosities of 10 wt% solutions of the individual branched-chain materials in the commercial mixture E7 were determined at 0 degree C and 20 degree C and substantial increases in the measured bulk viscosities were recorded.
