79544-29-9 Usage
Uses
Used in Pharmaceutical Industry:
2-Fluoro-6-iodobenzonitrile is used as a key intermediate in the synthesis of pharmaceutical compounds for its ability to enhance the properties of the final product, such as increasing lipophilicity and metabolic stability.
Used in Agrochemical Industry:
2-Fluoro-6-iodobenzonitrile is used as a building block in the development of agrochemicals, contributing to the creation of more effective and targeted pesticides and herbicides.
Used in Material Science:
2-Fluoro-6-iodobenzonitrile is utilized in the synthesis of advanced materials, such as polymers and coatings, where its fluorinated nature can impart specific properties like increased durability and resistance to environmental factors.
Used in Research and Development:
2-Fluoro-6-iodobenzonitrile serves as a valuable research tool in the development of new chemical entities and the study of structure-activity relationships in various fields, including medicinal chemistry and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 79544-29-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,5,4 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 79544-29:
(7*7)+(6*9)+(5*5)+(4*4)+(3*4)+(2*2)+(1*9)=169
169 % 10 = 9
So 79544-29-9 is a valid CAS Registry Number.
InChI:InChI:1S/C7H3FIN/c8-6-2-1-3-7(9)5(6)4-10/h1-3H
79544-29-9Relevant academic research and scientific papers
Super acid catalysed sequential hydrolysis/cycloisomerization of o-(acetylenic)benzamides under microwave condition: Synthesis, antinociceptive and antiinflammatory activity of substituted isocoumarins
Praveen, Chandrasekaran,Dheenkumar,Perumal
, p. 71 - 83 (2013/05/09)
Synthesis of isocoumarins and related compounds via triflic acid promoted hydrolysis/cyclization sequence of 2-(alkynyl)benzamides under microwave condition was achieved. The substrate scope of the reaction was broad to include not only aromatic but also
Direct Synthesis of 2,4-Diaminoquinazolines from 2-Fluorobenzonitriles
Hynes, John B.,Pathak, Alpana,Panos, Constantina H.,Okeke, Claudia C.
, p. 1173 - 1177 (2007/10/02)
In a search for new methods for preparing 2,4-diaminoquinazolines having a diversity of substituents in the benzenoid ring, it was found that the reaction of 2,6-difluorbenzonitrile with guanidine carbonate gave 2,4-diamino-5-fluoroquinazoline in excellent yield.Extension of this approach to other 2-fluorobenzonitriles, some of which were elaborated for the first time, showed that this reaction possesses considerable generality.The cyclization was sucessful even when electron donating groups were present at position six.Only in two cases where a primary or secondary amino group was also present ortho to the cyano group was this transformation unsucessful.
