181526-16-9 Usage
Uses
Used in Organic Synthesis:
Furo[2,3-b]pyridine, 7-oxide (9CI) serves as a crucial intermediate in organic synthesis, facilitating the creation of a variety of complex organic molecules.
Used in Pharmaceutical Development:
In the pharmaceutical industry, Furo[2,3-b]pyridine, 7-oxide (9CI) is utilized as a building block for the preparation of diverse medicinal compounds, contributing to the advancement of new treatments and therapies.
Used in Agrochemical Production:
Furo[2,3-b]pyridine, 7-oxide (9CI) also plays a significant role in agrochemical production, where it is employed as a component in the synthesis of various agricultural chemicals.
Used in Biological Research:
Furo[2,3-b]pyridine, 7-oxide (9CI) is used in biological research as an anti-inflammatory, anti-cancer, and anti-viral agent, aiding in the study and development of potential new drugs and therapies.
Used in Environmental Science:
In environmental science, the compound is investigated for its persistence and potential for bioaccumulation to assess its impact on ecosystems and ensure the safety of its applications.
Check Digit Verification of cas no
The CAS Registry Mumber 181526-16-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,1,5,2 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 181526-16:
(8*1)+(7*8)+(6*1)+(5*5)+(4*2)+(3*6)+(2*1)+(1*6)=129
129 % 10 = 9
So 181526-16-9 is a valid CAS Registry Number.
181526-16-9Relevant academic research and scientific papers
Furopyridines. XIX [1]. Reaction of furo[2,3-b]-, -[3,2-b]-, -[2,3-c]- and -[3,2-c]pyridine with acetic anhydride
Shiotani, Shunsaku,Taniguchi, Katsunori,Ishida, Toshimasa,In, Yasuko
, p. 647 - 654 (2007/10/03)
Acetoxylation of N-oxide of furo[2,3-b]- 2a, -[3,2-b]- 2b, -[2,3-c]- 2c and -[3,2-c]pyridine 2d with acetic anhydride afforded compounds substituted normally at the α- or γ-position to the ring nitrogen, 3a, 4a, 4b, 3d, 4d, 8 and 9, and in addition compounds substituted on the furan ring, 5a, 6a, 5b, 6b, 7b, 5c and 7c which were unexpected compounds. The structures of these compounds were established from the ir, nmr and mass spectra, and x-ray crystal analysis of 5b.
