132350-29-9 Usage
Uses
Used in Pharmaceutical Industry:
1,3,2-Dioxaborinane, 2-(3-phenylpropyl)is used as a reagent for the synthesis of various organic compounds, which are essential in the development of pharmaceutical products. Its ability to facilitate carbon-carbon bond formation makes it a valuable component in the production of biologically active molecules, contributing to the advancement of new drug candidates.
Used in Agrochemical Industry:
In the agrochemical sector, 1,3,2-Dioxaborinane, 2-(3-phenylpropyl)is employed as a reagent for the synthesis of organic compounds used in the production of agrochemicals. Its role in creating carbon-carbon bonds is crucial for the development of effective crop protection agents and other agricultural products.
Used in Materials Science:
1,3,2-Dioxaborinane, 2-(3-phenylpropyl)is used as a ligand for metal catalysts in organic transformations within the field of materials science. This application allows for the creation of new materials with improved properties, such as enhanced stability or reactivity, which can be utilized in various industrial applications.
Used in Organic Synthesis:
As a reagent in organic synthesis, 1,3,2-Dioxaborinane, 2-(3-phenylpropyl)is used for the formation of carbon-carbon bonds, which is a fundamental aspect of creating complex organic molecules. This makes it an essential tool in the synthesis of a wide range of chemical compounds, from simple organic molecules to more complex structures with potential applications in various industries.
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.
Organoboranes. 54. Exploration of the reactions of (α-haloallyl)lithium with organoborane derivatives. Simple and convenient procedure for the synthesis of three-carbon homologated boronate esters and terminal alkenes
Brown, Herbert C.,Rangaishenvi, Milind V.,Jayaraman, Seetharaman
, p. 1948 - 1954 (2008/10/08)
The synthetic utility of (α-haloallyl)lithium generated in situ for the facile transfer reaction of various organoborane derivatives, such as R3B, R2BOR′, and RB(OR′)2, has been explored. This has led to the synthesis of α-vinylboronate esters, RCH(CH=CH2)B(OR′)2. which are readily isomerized thermally to the corresponding allylboronate esters with the boron atom on the less substituted carbon atom, RCH= CHCH2B(OR′)2. Catalytic hydrogenation of these allylboronate esters furnishes saturated boronate esters, RCH2CH2CH2B(OR′)2, providing a three-carbon homologation of the original R-B2CH=CH2.
