186093-87-8 Usage
General Description
2-(4-Bromobenzoyl)-1-benzofuran-5-carbaldehyde is a chemical compound with the molecular formula C15H9BrO3. It is a benzofuran derivative with a bromobenzoyl group attached to the benzofuran ring. 2-(4-BROMOBENZOYL)-1-BENZOFURAN-5-CARBALDEHYDE is often used in organic synthesis and medicinal chemistry as a building block for creating various molecules with biological activity. Its structure and properties make it suitable for various applications in the field of pharmaceuticals, agrochemicals, and material science. The compound's unique combination of aromatic and aldehyde functional groups makes it a valuable reagent in the synthesis of complex molecules and pharmaceutical intermediates.
Check Digit Verification of cas no
The CAS Registry Mumber 186093-87-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,6,0,9 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 186093-87:
(8*1)+(7*8)+(6*6)+(5*0)+(4*9)+(3*3)+(2*8)+(1*7)=168
168 % 10 = 8
So 186093-87-8 is a valid CAS Registry Number.
InChI:InChI=1/C16H9BrO3/c17-13-4-2-11(3-5-13)16(19)15-8-12-7-10(9-18)1-6-14(12)20-15/h1-9H
186093-87-8Relevant articles and documents
Synthetic approaches to benzofuran containing Insulin Sensitivity Enhancer compounds for treatment of type II diabetes
Huff, Bret E.,Leffelman, Cindy L.,LeTourneau, Michael E.,Sullivan, Kevin A.,Ward, Jeffrey A.,Stille, John R.
, p. 1363 - 1384 (2007/10/03)
The search for Insulin Sensitivity Enhancer (ISE) compounds, for potential use in the treatment of Type II diabetes, has led to the synthesis of compounds that contain a benzofuran spacer between an aryloyl substituent and a 2,4-thiazolidinedione pharmacophore. Sequential combination of haloacetyl aryl substrates with 5-formylsalicylaldehyde gave the desired 2-aryloyl-5-formylbenzofuran intermediates. A related class of compounds, those with a methylene tether between the aromatic moiety and the benzofuran spacer, were also prepared through this strategy.
