948592-91-4 Usage
Uses
Used in Organic Synthesis:
(8-methylnaphthalen-1-yl)boronic acid is used as a reagent for forming carbon-carbon and carbon-heteroatom bonds in organic synthesis. Its ability to form complexes with diols and other Lewis bases makes it a valuable tool in creating a variety of organic compounds.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, (8-methylnaphthalen-1-yl)boronic acid is used as an intermediate for the synthesis of various drugs. Its unique reactivity allows for the development of new pharmaceutical compounds with potential therapeutic applications.
Used in Material Science:
(8-methylnaphthalen-1-yl)boronic acid is also used as a building block in the development of new materials with specific properties. Its incorporation into material science research can lead to the creation of advanced materials for various applications, such as electronics, coatings, and adhesives.
Check Digit Verification of cas no
The CAS Registry Mumber 948592-91-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,8,5,9 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 948592-91:
(8*9)+(7*4)+(6*8)+(5*5)+(4*9)+(3*2)+(2*9)+(1*1)=234
234 % 10 = 4
So 948592-91-4 is a valid CAS Registry Number.
948592-91-4Relevant academic research and scientific papers
Through-Space Shielding Effects of Metal-Complexed Phenyl Rings
Miles, William H.,Robinson, Michael J.,Lessard, Samantha G.,Thamattoor, Dasan M.
, p. 10791 - 10801 (2016/11/29)
Several naphthalene compounds containing a methyl group in a 1,8-relationship to a metal-complexed phenyl ring bearing various substituents have been synthesized. The through-space shielding effects of the phenyl ring, as a function of substituent and com
