193624-86-1 Usage
Uses
Used in Pharmaceutical Industry:
4-Chloro-furo[2,3-b]pyridine is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 4-chloro-furo[2,3-b]pyridine serves as an intermediate for the production of agrochemicals, contributing to the development of effective pesticides and other agricultural chemicals.
Used in Chemical Materials Development:
4-Chloro-furo[2,3-b]pyridine is utilized in the development of novel chemical materials, thanks to its reactive functional groups and structural properties that can be tailored for specific applications.
Used in Organic Synthesis:
As a building block in organic synthesis, 4-chloro-furo[2,3-b]pyridine is employed to construct complex organic molecules for research and industrial purposes, expanding the scope of chemical compounds available for various uses.
Used in Medicinal Chemistry Research:
4-Chloro-furo[2,3-b]pyridine holds potential for exhibiting diverse biological activities, making it a valuable compound for researchers in medicinal chemistry to explore its properties and applications in drug discovery.
Used in Pharmacology Studies:
In pharmacology, 4-chloro-furo[2,3-b]pyridine is of interest for its potential to interact with biological targets, providing insights into its therapeutic effects and mechanisms of action, which can guide the design of new pharmaceutical agents.
Check Digit Verification of cas no
The CAS Registry Mumber 193624-86-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,6,2 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 193624-86:
(8*1)+(7*9)+(6*3)+(5*6)+(4*2)+(3*4)+(2*8)+(1*6)=161
161 % 10 = 1
So 193624-86-1 is a valid CAS Registry Number.
193624-86-1Relevant academic research and scientific papers
Shiotani, Shunsaku,Taniguchi, Katsunori
, p. 925 - 929 (1997)
Chlorination of the N-oxides of furo[2,3-b]- 1a, -[2,3-c]- 1b and -[3,2-c]pyridine 1c with phosphorus oxychloride afforded compounds substituted normally at the α- or γ-position to the ring nitrogen, 2a, 2′a, 2b, 2c, 2′c and 2″c, and in addition, in the case of 1b, compounds substituted on the furan ring, 2′b and 2″b. The structures of these compounds were confirmed from their ir, nmr and mass spectra. The major chlorinated products 2a, 2b and 2c were converted to methoxy- 5a, 5b and 5c, N-pyrrolidyl- 7a, 7b and 7c, and phenylthiofuropyridines 8a, 8b, and 8c.
