1315692-91-1 Usage
Uses
Used in Organic Synthesis:
2,6-difluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline is used as a synthetic intermediate for the preparation of various organic compounds. Its unique structure allows for versatile chemical reactions, making it a valuable component in the synthesis of complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2,6-difluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline is used as a building block for the design and development of new pharmaceuticals. Its unique chemical properties can contribute to the creation of novel drug candidates with improved therapeutic properties.
Used in Materials Science:
2,6-difluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline is also used in materials science for the development of new materials with specific properties. Its incorporation into various materials can lead to the creation of innovative products with applications in different industries.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 2,6-difluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline is used as a key component in the synthesis of new drugs. Its unique structure can contribute to the development of drugs with enhanced efficacy and selectivity, potentially leading to improved treatments for various diseases.
Used in Agrochemicals:
2,6-difluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline is also utilized in the agrochemical industry for the development of new pesticides and other agricultural chemicals. Its unique chemical properties can be harnessed to create more effective and environmentally friendly products.
It is important to handle and use 2,6-difluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline with caution, following proper safety guidelines and regulations to ensure the safety of researchers and industrial manufacturers.
Check Digit Verification of cas no
The CAS Registry Mumber 1315692-91-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,5,6,9 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1315692-91:
(9*1)+(8*3)+(7*1)+(6*5)+(5*6)+(4*9)+(3*2)+(2*9)+(1*1)=161
161 % 10 = 1
So 1315692-91-1 is a valid CAS Registry Number.
1315692-91-1Relevant academic research and scientific papers
Preparation of 2-fluoro-3-aminophenylboronates via directed ortho -metalation
Zhichkin, Paul E.,Krasutsky, Sergiy G.,Beer, Catherine M.,Rennells, W. Martin,Lee, Seung H.,Xiong, Jin-Ming
, p. 1604 - 1608 (2011/06/25)
The aromatic amine in fluoroanilines was protected with 2,2,5,5-tetramethyl-1-aza-2,5-disila-cyclopentane (stabase) in order to direct metalation ortho to the fluorine. A series of novel 2-fluoro-3- aminophenylboronates were prepared after quenching the metalated intermediate with triisopropylborate and deprotection in situ. The presented method is convenient and scalable, because all of the synthetic steps use crude intermediates. Several transformations are carried out in the same pot, and the final boronates are easily purified crystalline materials. Georg Thieme Verlag Stuttgart · New York.
