107096-03-7 Usage
General Description
Furo[3,2-b]pyridin-3(2H)-one,2-methyl-(9CI) is a chemical compound categorized under the class of organic compounds known as pyridinones and derivatives. The primary use of this chemical is not well-documented, indicating its potential application in various experimental or industrial processes. Its characteristics such as melting point, boiling point, density, etc. are not specified, hence, caution is advised while handling or storing this chemical. Potential hazards and health effects of exposure to this chemical are also not well studied, highlighting the need for further investigation into risks associated with this compound. The compound's exact structure suggests it contains a furo pyridinone ring, with a methyl group attached, and its complete name suggests it is the 9th compound in a series (9CI).
Check Digit Verification of cas no
The CAS Registry Mumber 107096-03-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,0,9 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 107096-03:
(8*1)+(7*0)+(6*7)+(5*0)+(4*9)+(3*6)+(2*0)+(1*3)=107
107 % 10 = 7
So 107096-03-7 is a valid CAS Registry Number.
107096-03-7Relevant articles and documents
Furopyridines.III.A New Synthesis of Furopyridine
Shiotani, Shunsaku,Morita, Hiroyuki
, p. 665 - 668 (2007/10/02)
A convenient synthesis of furopyridine and its 2- and 3-methyl derivatives from ethyl 3-hydroxypicolinate (1) is described.The hydroxy ester 1 was O-alkylated with ethyl bromoacetate or ethyl 2-bromopropionate to give the diester 2a or 2b.Cyclization of compound 2a afforded ethyl 3-hydroxyfuropyridine-2-carboxylate (3) which in turn was hydrolyzed and decarboxylated to give furopyridin-3-(2H)-one (4a).Cyclization of 2b gave the 2-methyl derivative 4b.Reduction of 4a and 4b with sodium borohydride yielded the corresponding hydroxy derivative 5a and 5b respectively, which were dehydrated with phosphoric acid to give furopyridine (6a) and its 2-methyl derivative (6b). 2-Acetylpyridin-3-ol (8) was converted to the ethoxycarbonylmethyl ether (9) by O-alkylation with ethyl bromoacetate, which was cyclized to give 3-methylfuropyridine-2-carboxylic acid (10).Decarboxylation of 10 afforded 3-methylfuropyridine (11).
