197024-83-2 Usage
Uses
Used in Organic Synthesis:
Thiophene-2-boronic acid, propanediol cyclic ester serves as a valuable building block in organic synthesis, contributing to the creation of complex organic molecules and facilitating various chemical reactions due to its unique structural features.
Used in Pharmaceutical Research:
In pharmaceutical research, Thiophene-2-boronic acid, propanediol cyclic ester is utilized as a pharmaceutical intermediate, playing a crucial role in the development of new drugs and therapeutic agents.
Used as a Ligand in Metal-Catalyzed Reactions:
Thiophene-2-boronic acid, propanediol cyclic ester has been investigated for its potential as a ligand in metal-catalyzed reactions, where it can enhance the efficiency and selectivity of these reactions, contributing to the advancement of synthetic methodologies.
Used in Antimicrobial Applications:
Thiophene-2-boronic acid, propanediol cyclic ester has demonstrated antimicrobial properties, making it a candidate for use in applications aimed at controlling or eliminating harmful microorganisms, which can be particularly relevant in the development of new antibiotics.
Used in Antifungal Applications:
Similarly, its antifungal properties position Thiophene-2-boronic acid, propanediol cyclic ester as a potential agent in combating fungal infections, offering a new avenue for treatment in medical and agricultural settings.
Used in Chemical Research:
In the broader field of chemical research, Thiophene-2-boronic acid, propanediol cyclic ester is employed for studying the fundamental properties of boronic acid derivatives and their interactions with other chemical entities, further expanding the understanding of chemical reactivity and bonding.
Check Digit Verification of cas no
The CAS Registry Mumber 197024-83-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,7,0,2 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 197024-83:
(8*1)+(7*9)+(6*7)+(5*0)+(4*2)+(3*4)+(2*8)+(1*3)=152
152 % 10 = 2
So 197024-83-2 is a valid CAS Registry Number.
197024-83-2Relevant academic research and scientific papers
Generation of organolithium compounds bearing super silyl ester and their application to Matteson rearrangement
Oda, Susumu,Yamamoto, Hisashi
supporting information, p. 8165 - 8168 (2013/08/23)
It's super-silyl-fragilithyl-ester-aryl-docious: The super silyl group is a strong protecting group for carboxylic acids and provides a method for direct lithiation that is compatible with the ester moiety. Organolithium compounds bearing a super silyl ester react with a variety of electrophiles in high yields (see scheme). The reaction of lithiated super silyl chloroacetate with a boron compound gives α-functionalization of the ester moiety by Matteson rearrangement. Copyright
A solution-processable deep red molecular emitter for non-doped organic red-light-emitting diodes
Wang, Zhiming,Lu, Ping,Xue, Shanfeng,Gu, Cheng,Lv, Ying,Zhu, Qing,Wang, Huan,Ma, Yuguang
experimental part, p. 356 - 363 (2012/06/18)
A new solution-processable deep red emitter, TCTzC, containing dithienylbenzothiadiazole unit and four alkyl-linked peripheral carbazole groups, is designed and synthesized in high yield by Suzuki coupling reaction. The four peripheral carbazole substituents enhance the hole-transport ability, glass transition temperature, decompose temperature and film forming ability of TCTzC. The single-layered device based on TCTzC shows saturated deep red electroluminescence with a CIE coordinate of (0.70, 0.30). The current efficiency and quantum efficiency of TCTzC is two times higher than the compound without the four peripheral carbazole groups. The higher device performance is obtained when TPBi is applied and the external quantum efficiency could reach to 0.93%.
