952149-27-8 Usage
Uses
Used in Organic Synthesis:
3-Vinylbenzo[c][1,2]oxaborol-1(3H)-ol is used as a reagent in organic synthesis for the formation of carbon-carbon and carbon-heteroatom bonds in various chemical reactions. Its unique structure and reactivity make it a valuable building block in this field.
Used in Material Development:
3-Vinylbenzo[c][1,2]oxaborol-1(3H)-ol is used as a precursor in the development of new materials, leveraging its boron-containing structure and reactivity to create novel materials with specific properties.
Used in Pharmaceutical Development:
3-Vinylbenzo[c][1,2]oxaborol-1(3H)-ol is used as a building block in the development of new pharmaceuticals, where its unique structure and reactivity can contribute to the creation of innovative drug candidates with potential therapeutic applications.
Used in Chemical Research:
3-Vinylbenzo[c][1,2]oxaborol-1(3H)-ol is used as a subject of study in chemical research to explore its properties, reactivity, and potential applications in various chemical processes and reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 952149-27-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,2,1,4 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 952149-27:
(8*9)+(7*5)+(6*2)+(5*1)+(4*4)+(3*9)+(2*2)+(1*7)=178
178 % 10 = 8
So 952149-27-8 is a valid CAS Registry Number.
952149-27-8Relevant academic research and scientific papers
PYRIMIDINE COMPOUNDS AS TUBERCULOSIS INHIBITORS
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, (2011/02/24)
The present invention relates to compounds II useful as inhibitors of treating tuberculosis. The invention also provides processes for preparing compounds of the invention.
Practical synthesis and applications of benzoboroxoles
Gunasekera, Dinara S.,Gerold, Dennis J.,Aalderks, Nathan S.,Chandra, J. Subash,Maanu, Christiana A.,Kiprof, Paul,Zhdankin, Viktor V.,Reddy, M. Venkat Ram
, p. 9401 - 9405 (2008/02/13)
A convenient one-pot synthesis of benzoboroxoles has been developed via the reaction of o-bromobenzyl alcohols with NaH, nBuLi, and B(OiPr)3 followed by acidic hydrolysis. Applications of these benzoboroxoles have been demonstrated in Pd-catalyzed cross-coupling reactions and the protocol has been extended for the synthesis of a chiral benzoboroxole. Exceptionally short synthesis of a potent antifungal agent AN2690 and several of its analogs has also been realized.
