301699-39-8 Usage
Uses
Different sources of media describe the Uses of 301699-39-8 differently. You can refer to the following data:
1. Reactant for:? ;Preparation of biologically and pharmacologically active molecules1,2? ;Suzuki and Stille cross-coupling reaction3? ;Mizoroki-Heck arylation4? ;Baeyer-Villiger oxidation5? ;Rhodium-catalyzed asymmetric conjugate addition reactions6
2. suzuki reaction
3. Reactant for:Preparation of biologically and pharmacologically active moleculesSuzuki and Stille cross-coupling reactionMizoroki-Heck arylationBaeyer-Villiger oxidationRhodium-catalyzed asymmetric conjugate addition reactions
Check Digit Verification of cas no
The CAS Registry Mumber 301699-39-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,1,6,9 and 9 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 301699-39:
(8*3)+(7*0)+(6*1)+(5*6)+(4*9)+(3*9)+(2*3)+(1*9)=138
138 % 10 = 8
So 301699-39-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H13BO3/c1-6-4-8(10(11)12)5-7(2)9(6)13-3/h4-5,11-12H,1-3H3
301699-39-8Relevant articles and documents
Formation of hetero-boroxines: Dynamic combinatorial libraries generated through trimerization of pairs of arylboronic acids
Tokunaga, Yuji,Ueno, Hiroki,Shimomura, Youji
, p. 219 - 223 (2008/09/17)
Condensation of pairs of arylboronic acids provided homo- and hetero-boroxines in solution as evidenced from NMR spectra, and those boroxines were detected in the gas phase by GC-MS spectrometry. Equilibrium constants for the formation of these boroxines in solution were obtained through integration of pertinent signals in the NMR spectra of the mixtures ofboronic acids.
