4844-17-1 Usage
Description
2,4,5-triphenyl-1,3,2-dioxaborole is a boron-containing chemical compound with the molecular formula C18H15BO2. It features a unique structure where three phenyl groups are attached to a boron atom, which endows it with distinctive reactivity and properties. 2,4,5-triphenyl-1,3,2-dioxaborole has garnered attention in the realm of organic synthesis, particularly for its role in the formation of carbon-carbon bonds.
Uses
Used in Organic Synthesis:
2,4,5-triphenyl-1,3,2-dioxaborole is utilized as a reagent in the Suzuki-Miyaura coupling reaction, a pivotal method for the formation of carbon-carbon bonds. Its application in this reaction is crucial for the synthesis of various organic compounds, highlighting its importance in the field of organic chemistry.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,4,5-triphenyl-1,3,2-dioxaborole is used as a key intermediate in the synthesis of complex organic molecules, including potential drug candidates. Its unique structure and reactivity facilitate the creation of new chemical entities with therapeutic potential.
Used in Material Science:
2,4,5-triphenyl-1,3,2-dioxaborole also finds applications in material science, where it is employed in the development of novel materials with specific properties. Its ability to form stable bonds with carbon atoms makes it a valuable component in the synthesis of advanced polymers and other materials with tailored characteristics for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 4844-17-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,4 and 4 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4844-17:
(6*4)+(5*8)+(4*4)+(3*4)+(2*1)+(1*7)=101
101 % 10 = 1
So 4844-17-1 is a valid CAS Registry Number.
InChI:InChI=1/C20H15BO2/c1-4-10-16(11-5-1)19-20(17-12-6-2-7-13-17)23-21(22-19)18-14-8-3-9-15-18/h1-15H
4844-17-1Relevant articles and documents
Neue Synthesen und Reaktionen ungesaettigter Heterotitanacyclen
Duerr, Stefan,Hoehlein, Udo,Schobert, Rainer
, p. 89 - 96 (2007/10/02)
Dicarbonyltitanocene reacts chemoselectively with difunctional carbonyl compounds such as 1,2-diketones and 1,4-diketo-2-enes, with α-ketothioketones, α-ketoimines and azodicarbonic esters and -amides to yield the corresponding, mostly new, heterotitanacycles that are capable of a lot of a useful follow-up reactions.These chelate complexes, containing three to four heteroatoms, allow the substitution of the entire titanocene fragment by carbon (formation of vinylenic carbonates and the thia-derivatives of these) or by further heteroatoms like boron or phosphorus(formation of boroles and phosphonic acid derivatives), thus retaining the cyclofunctionality.Alternatively, some of the new chelate complexes can be readily C-C-chain-lengthened via a deprotonating/alkylating sequence, leaving the metallacycle unaffected.
Conversion of Benzoin into 9,10-Phenanthrenequinone by Photocyclisation
de Vries, Johannes G.,Hubbard, Sally A.
, p. 1172 - 1173 (2007/10/02)
Benzoin is converted into 9,10-phenanthrenequinone by photocyclisation of its adduct with phenylboric acid, followed by hydrolysis of the photoproduct.
