132350-29-9 Usage
General Description
1,3,2-Dioxaborinane, 2-(3-phenylpropyl)- is a chemical compound with the molecular formula C11H15BO2. It is a boron-based compound that is commonly used in organic synthesis as a reagent for the formation of carbon-carbon bonds. 1,3,2-Dioxaborinane, 2-(3-phenylpropyl)- has a boron atom that is bound to two oxygen atoms and a phenylpropyl group, which makes it useful for various chemical reactions such as Suzuki-Miyaura coupling and palladium-catalyzed cross-coupling reactions. It is often used in the pharmaceutical and agrochemical industries for the production of various organic compounds and has shown potential as a building block for the synthesis of biologically active molecules. Additionally, it has applications in the field of materials science and can be used as a ligand for metal catalysts in organic transformations.
Check Digit Verification of cas no
The CAS Registry Mumber 132350-29-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,3,5 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 132350-29:
(8*1)+(7*3)+(6*2)+(5*3)+(4*5)+(3*0)+(2*2)+(1*9)=89
89 % 10 = 9
So 132350-29-9 is a valid CAS Registry Number.
132350-29-9Relevant articles and documents
Palladium-catalyzed borylation of primary alkyl bromides
Joshi-Pangu, Amruta,Ma, Xinghua,Diane, Mohamed,Iqbal, Sidra,Kribs, Robert J.,Huang, Richard,Wang, Chao-Yuan,Biscoe, Mark R.
, p. 6629 - 6633 (2012)
A mild Pd-catalyzed process for the borylation of alkyl bromides has been developed using bis(pinacolato)diboron as a boron source. This process accommodates the use of a wide range of functional groups on the alkyl bromide substrate. Primary bromides react with complete selectivity in the presence of a secondary bromide. The generality of this approach is demonstrated by its extension to the use of alkyl iodides and alkyl tosylates, as well as borylation reactions employing bis(neopentyl glycolato)diboron as the boron source.
