230299-21-5 Usage
Uses
Different sources of media describe the Uses of 230299-21-5 differently. You can refer to the following data:
1. suzuki reaction
2. Bis(hexylene glycolato)diboron can be used as a reagent: To prepare aryl boronate esters via metal-catalyzed direct C-H borylation of aryl compounds. In the chemoselective synthesis of C?C coupling products via nickel catalyzed coupling of primary and secondary alkyl halides. In the nickel-catalyzed regioselective arylboration of terminal nonactivated alkenes to yield alkyl boranes.
Check Digit Verification of cas no
The CAS Registry Mumber 230299-21-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,0,2,9 and 9 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 230299-21:
(8*2)+(7*3)+(6*0)+(5*2)+(4*9)+(3*9)+(2*2)+(1*1)=115
115 % 10 = 5
So 230299-21-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H24B2O4/c1-9-7-11(3,4)17-13(15-9)14-16-10(2)8-12(5,6)18-14/h9-10H,7-8H2,1-6H3
230299-21-5Relevant articles and documents
A process for preparing a diboron ester (by machine translation)
-
Paragraph 0016, (2016/12/16)
The invention discloses a process for preparing a diboron ester. Borane complexes and corresponding diol reaction and produce corresponding mellow borane, the iron then took place in the presence of catalyst to self-coupling forming a diboron ester. Short synthesis steps of the method, high safety, mild reaction conditions, suitable for many kinds of a diboron ester synthesis. (by machine translation)
PREPARATION OF DIBORONIC ESTERS
-
Page 15, (2008/06/13)
This invention relates to a process for the preparation of an ester of diboronic acid comprising reacting a tetrakis(dialkylamino)diboron with an alcohol to form the ester and a volatile dialkylamine, wherein the volatile dialkylamine is liberated from the reaction mixture in gaseous form.
