88978-20-5 Usage
General Description
3-(2,2,2-trifluoroacetamido)benzeneboronic acid is a chemical compound containing a boronic acid substituent attached to a benzene ring and a trifluoroacetamido group. It is often used as a building block in organic synthesis and as a reagent in the preparation of pharmaceuticals and other biologically active compounds. 3-(2,2,2-TRIFLUOROACETAMIDO)BENZENEBORONIC ACID is known for its ability to form stable complexes with diols, making it useful in the development of selective sensors and drug delivery systems. Additionally, the trifluoroacetamido group enhances the compound's stability and solubility, making it a versatile and valuable tool for researchers and chemists in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 88978-20-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,9,7 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 88978-20:
(7*8)+(6*8)+(5*9)+(4*7)+(3*8)+(2*2)+(1*0)=205
205 % 10 = 5
So 88978-20-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H7BF3NO3/c10-8(11,12)7(14)13-6-3-1-2-5(4-6)9(15)16/h1-4,15-16H,(H,13,14)
88978-20-5Relevant articles and documents
Synthesis of diverse β-quaternary ketones via palladium-catalyzed asymmetric conjugate addition of arylboronic acids to cyclic enones
Holder, Jeffrey C.,Goodman, Emmett D.,Kikushima, Kotaro,Gatti, Michele,Marziale, Alexander N.,Stoltz, Brian M.
, p. 5781 - 5792 (2015/08/03)
Abstract The development and optimization of a palladium-catalyzed asymmetric conjugate addition of arylboronic acids to cyclic enone conjugate acceptors is described. These reactions employ air-stable and readily-available reagents in an operationally si
