170938-13-3 Usage
Uses
Used in Organic Synthesis:
α-Vinyl-(4-phenyl-phenyl)methanol is utilized as a key intermediate in the synthesis of various organic molecules. Its unique structure allows for the creation of a diverse array of chemical products, contributing to the advancement of organic chemistry.
Used in Pharmaceutical Development:
α-vinyl-(4-phenyl-phenyl)methanol is employed as a precursor in the development of pharmaceuticals. Its potential biological activities make it a valuable asset in the discovery and synthesis of new drugs, potentially leading to breakthroughs in medicine.
Used in Materials Science:
In the field of materials science, α-vinyl-(4-phenyl-phenyl)methanol is used as a building block for the development of polymers and other advanced materials. Its incorporation into these materials can enhance their properties, such as strength, flexibility, or chemical resistance, depending on the specific application.
Used in Polymer Development:
α-Vinyl-(4-phenyl-phenyl)methanol is used as a monomer in the synthesis of polymers. Its vinyl group allows for polymerization reactions, resulting in polymers with tailored properties for specific industrial applications, such as coatings, adhesives, or plastics.
Used in Advanced Material Research:
α-vinyl-(4-phenyl-phenyl)methanol is also used in the research and development of advanced materials, where its unique structure and properties can contribute to the creation of innovative materials with enhanced performance characteristics for various high-tech applications.
Check Digit Verification of cas no
The CAS Registry Mumber 170938-13-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,0,9,3 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 170938-13:
(8*1)+(7*7)+(6*0)+(5*9)+(4*3)+(3*8)+(2*1)+(1*3)=143
143 % 10 = 3
So 170938-13-3 is a valid CAS Registry Number.
170938-13-3Relevant academic research and scientific papers
Wang, Zhihui,Fang, Hongyun,Xi, Zhenfeng
, p. 499 - 501 (2005)
Lithiation of 1-bromo-4-trisubstituted silyl-1,3-butadiene derivatives with t-BuLi afforded substituted siloles in high yields. Cleavage of one of the three C-Si bonds took place via intramolecular nucleophilic substitution. Selective cleavage was observed when the silyl group possessed different substituents. Results showed that vinyl and phenyl substituents on Si were substituted much more easily than methyl groups, whilst a methyl group was exclusively deleted from an i-Pr-SiMe2 moiety.
