132350-07-3 Usage
Type of compound
Boron-containing heterocyclic compound
Potential applications
a. Organic synthesis
b. Reagent in the formation of carbon-carbon bonds
Common use
a. Suzuki-Miyaura coupling reaction
b. Formation of biaryl compounds
Utilization
a. Preparation of functionalized compounds
b. Pharmaceutical industry
c. Agrochemicals
d. Materials science
These properties and applications highlight the versatility and importance of 1,3,2-Dioxaborinane, 2-[1-(phenylmethyl)-2-propenyl]in various fields of chemistry and research.
Check Digit Verification of cas no
The CAS Registry Mumber 132350-07-3 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, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 132350-07:
(8*1)+(7*3)+(6*2)+(5*3)+(4*5)+(3*0)+(2*0)+(1*7)=83
83 % 10 = 3
So 132350-07-3 is a valid CAS Registry Number.
132350-07-3Relevant academic research and scientific papers
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.
