193750-68-4 Usage
Uses
Used in Organic Chemistry:
Ethanone, 1-furo[2,3-b]pyridin-6-yl(9CI) is used as a building block for the synthesis of other organic compounds. Its unique structure, which includes a furan ring fused to a pyridine ring and a ketone functional group, allows for the creation of a variety of complex molecules with potential applications in various fields.
Used in Medicinal Chemistry:
Ethanone, 1-furo[2,3-b]pyridin-6-yl(9CI) is used as a potential candidate for the development of new pharmaceuticals. Its structure may exhibit biological activity, making it a valuable starting point for the design and synthesis of novel drugs. Further research is required to explore its potential therapeutic applications and to optimize its properties for use in medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 193750-68-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,7,5 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 193750-68:
(8*1)+(7*9)+(6*3)+(5*7)+(4*5)+(3*0)+(2*6)+(1*8)=164
164 % 10 = 4
So 193750-68-4 is a valid CAS Registry Number.
193750-68-4Relevant academic research and scientific papers
Furopyridines, XXII [1]. Elaboration of the C-Substituents alpha to the Heteronitrogen Atom of Furo[2,3-b] -, -[3,2-6] -, -[2,3-c]- and -[3,2-c]pyridine
Shiotani, Shunsaku,Tanigochi, Katsunori
, p. 901 - 907 (2007/10/03)
The Grignard reaction of fused ring cyanopyridine derivatives 1a-d with methyl- and phenylmagnesium bromide yielded the corresponding acylpyridine compounds 2a-d and 3a-d. Furopyridine N-oxides 4a-d were converted into the compounds having a phenyl group at the α-position to the ring nitrogen 5a-d. Reduction of 1a-d and the carboxylic esters 6a-d with diisobutylaluminium hydride yielded the corresponding amines 7a-d and aldehydes 9a-d. The aldehydes were converted to nitroethanol derivatives 10a-d by condensation with nitromethane and acrylic ester compounds 11a-d by the Wittig-Horner reaction with methyl diethyl phosphonoacetate.
