1029684-36-3 Usage
Uses
Used in Organic Synthesis:
2-Chloro-1-(tetrahydro-2H-pyran-2-yl)-1H-imidazole-5-boronic acid pinacol ester is used as a synthetic intermediate for the development of various organic compounds. Its unique structure allows for further functionalization and modification, making it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Chloro-1-(tetrahydro-2H-pyran-2-yl)-1H-imidazole-5-boronic acid pinacol ester is used as a key component in the development of novel drug candidates. Its versatile chemical properties enable the creation of new molecules with potential therapeutic applications, targeting a wide range of diseases and conditions.
Used in Material Science:
2-Chloro-1-(tetrahydro-2H-pyran-2-yl)-1H-imidazole-5-boronic acid pinacol ester is also utilized in the field of material science for the development of advanced materials with specific properties. Its unique structure can be exploited to create new materials with improved performance characteristics, such as enhanced stability, reactivity, or selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 1029684-36-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,9,6,8 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1029684-36:
(9*1)+(8*0)+(7*2)+(6*9)+(5*6)+(4*8)+(3*4)+(2*3)+(1*6)=163
163 % 10 = 3
So 1029684-36-3 is a valid CAS Registry Number.
1029684-36-3Relevant academic research and scientific papers
A new boronic-acid based strategy to synthesize 4(5)-(het)aryl-1H-imidazoles
Primas, Nicolas,Mahatsekake, Clément,Bouillon, Alexandre,Lancelot, Jean-Charles,Oliveira Santos, Jana Sopkovà-de,Lohier, Jean-Fran?ois,Rault, Sylvain
, p. 4596 - 4601 (2008/09/20)
This paper describes the synthesis of a new N-THP protected 5-(1H)-imidazolyl boronic acid pinacol ester and its use in Suzuki cross-coupling reactions with a wide range of (het)aryl halides to provide 4(5)-(het)aryl-1H-imidazoles.
