850568-72-8 Usage
Description
4-(TERT-BUTOXYCARBONYL)PHENYLBORONIC ACID is a boronic acid derivative featuring a tert-butoxycarbonyl (Boc) protecting group. This chemical compound is widely recognized for its utility in organic synthesis and pharmaceutical research, serving as a valuable building block for the creation of diverse organic molecules. Its unique structure and reactivity contribute to its status as a versatile and significant reagent within the realm of organic chemistry.
Uses
Used in Organic Synthesis:
4-(TERT-BUTOXYCARBONYL)PHENYLBORONIC ACID is used as a key intermediate for the synthesis of various organic molecules, leveraging its reactivity and the protective Boc group to facilitate complex molecular constructions.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 4-(TERT-BUTOXYCARBONYL)PHENYLBORONIC ACID is utilized as a component in the development of potential drug candidates, targeting a range of diseases. Its incorporation into drug molecules can enhance their pharmacological properties and therapeutic potential.
Used in the Suzuki-Miyaura Coupling Reaction:
A prominent application of 4-(TERT-BUTOXYCARBONYL)PHENYLBORONIC ACID is in the Suzuki-Miyaura coupling reaction, where it serves as a reactant to form carbon-carbon bonds. This reaction is pivotal for constructing the molecular frameworks of numerous organic compounds, including those with pharmaceutical relevance.
Overall, 4-(TERT-BUTOXYCARBONYL)PHENYLBORONIC ACID's applications cut across multiple industries, underscoring its importance in both the creation of novel organic compounds and the advancement of pharmaceutical agents.
Check Digit Verification of cas no
The CAS Registry Mumber 850568-72-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,0,5,6 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 850568-72:
(8*8)+(7*5)+(6*0)+(5*5)+(4*6)+(3*8)+(2*7)+(1*2)=188
188 % 10 = 8
So 850568-72-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H15BO4/c1-11(2,3)16-10(13)8-4-6-9(7-5-8)12(14)15/h4-7,14-15H,1-3H3
850568-72-8Relevant articles and documents
3D-printed cartridge system for in-flow photo-oxygenation of 7-aminothienopyridinones
Rastelli, Ettore J.,Yue, Doris,Millard, Caroline,Wipf, Peter
supporting information, (2020/12/29)
A 3D-printed polypropylene (PP) continuous-photoflow cell based on a modular cartridge system was developed for the photo-oxygenation of 7-aminothieno[3,2-c]pyridin-4(5H)-ones, using ambient air as the sole co-reactant. This strategy takes advantage of the versatility of 3D-printing to construct cost-effective meso-scale reactors. In addition to scalability, a short residence time (tR 2 min) in 100-W blue LED light that minimizes the formation of dark, insoluble decomposition products is a tangible benefit of this technology.
Competing dehalogenation versus borylation of aryl iodides and bromides under transition-metal-free basic conditions
Niu, Yi-Jie,Sui, Guo-Hui,Zheng, Hong-Xing,Shan, Xiang-Huan,Tie, Lin,Fu, Jia-Le,Qu, Jian-Ping,Kang, Yan-Biao
, p. 10805 - 10813 (2019/09/30)
In this work, selectivity-controllable base-promoted transition-metal-free borylation and dehalogenation of aryl halides are described. Under the conditions of borylation, the dehalogenation which emerges as a competitive side reaction has been well-controlled by carefully controlling the borylation conditions. On the other hand, the dehalogenation using benzaldehyde as a hydrogen source has also been accomplished. The applications of direct radical borylation and dehalogenation of aryl halides demonstrate their synthetic practicability in pharmaceutical-oriented organic synthesis. Based on the experimental evidences, the tBuOK/1,10-Phen-triggered radical nature of both competitive reactions has been revealed.
METHODS OF MANUFACTURING OF BORON COMPOUND WITHOUT TRANSITION METALS
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Paragraph 0065; 0066; 0071; 0072; 0076, (2018/05/03)
The present invention refers to aryl boron compound number bath method relates to search, more particularly transition metal catalyst to a tank without the use of boron compounds number is given to the aryl organic halo [ceyn [ceyn] freight method are disclosed to boron. (by machine translation)
