159870-80-1 Usage
Uses
Used in Pharmaceutical Industry:
5-Fluoro-2-Iodopyridine is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique chemical structure allows for the development of new drugs with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, 5-Fluoro-2-Iodopyridine serves as a versatile building block for the creation of more complex organic molecules. Its reactivity and structural features make it suitable for various synthetic routes and reactions.
Used in Research and Development:
5-Fluoro-2-Iodopyridine is utilized in research and development settings to explore its chemical properties and potential applications. Scientists and researchers use 5-FLUORO-2-IODOPYRIDINE to study its reactivity, stability, and interactions with other molecules, paving the way for new discoveries and innovations.
Safety Precautions:
Due to its potential harmful effects, 5-Fluoro-2-Iodopyridine should be handled with appropriate safety measures. It is available in solid form and can be hazardous if swallowed, inhaled, or comes in contact with skin or eyes. Proper handling, storage, and disposal procedures should be followed to minimize risks.
Chemical Abstracts Service (CAS) Number:
The CAS number for 5-Fluoro-2-Iodopyridine is 40745-80-8, which is a unique identifier used in chemical databases and literature to facilitate accurate referencing and communication of 5-FLUORO-2-IODOPYRIDINE.
Check Digit Verification of cas no
The CAS Registry Mumber 159870-80-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,8,7 and 0 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 159870-80:
(8*1)+(7*5)+(6*9)+(5*8)+(4*7)+(3*0)+(2*8)+(1*0)=181
181 % 10 = 1
So 159870-80-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H3FIN/c6-4-1-2-5(7)8-3-4/h1-3H
159870-80-1Relevant academic research and scientific papers
Oxadiazolopyridine Derivates for Use as Ghrelin O-Acyl Transferase (GOAT) Inhibitors
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Paragraph 0249-0253; 0271-0274, (2018/03/01)
The present invention relates to compounds of general formula I, wherein the groups R1, R2 and n are defined as in claim 1, which have valuable pharmacological properties, in particular bind to ghrelin O-acyl transferase (GOAT) and modulate its activity. The compounds are suitable for treatment and prevention of diseases which can be influenced by this receptor, such as metabolic diseases, in particular obesity.
Copper-catalyzed conversion of aryl and heteroaryl bromides into the corresponding iodide
Feng, Xiujuan,Li, Lingyu,Yu, Xiaoqiang,Yamamoto, Yoshinori,Bao, Ming
, p. 129 - 132 (2016/07/06)
An efficient method for the synthesis of aryl and heteroaryl iodides is described in this study. The reactions of aryl and heteroaryl bromides with potassium iodide proceeded smoothly in the presence of a copper catalyst under mild reaction conditions to produce the corresponding iodides in satisfactory to excellent yields.
