170938-13-3 Usage
General Description
α-vinyl-(4-phenyl-phenyl)methanol is a chemical compound with the molecular formula C15H14O. It is a derivative of benzyl and phenyl, and it contains a vinyl group. α-vinyl-(4-phenyl-phenyl)methanol is commonly used in the synthesis of various organic molecules and pharmaceuticals. It is also known for its potential applications in the field of materials science, particularly in the development of polymers and other advanced materials. α-vinyl-(4-phenyl-phenyl)methanol may also have biological activities and could be studied for its potential pharmaceutical properties. Overall, this compound has diverse uses and applications in various scientific and industrial fields.
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 articles and documents
Cleavage of C-Si bond by intramolecular nucleophilic attack: Lithiation-promoted formation of siloles from 1-bromo-4-trisubstituted silyl-1,3-butadiene derivatives
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.
