244221-04-3 Usage
Description
Benzene, 1-fluoro-4-(2-isocyanoethyl)(9CI) is a chemical compound characterized by the molecular formula C9H7FN. It is a benzene derivative featuring a fluoride atom at the 1 position and a 2-isocyanoethyl group at the 4 position. Benzene, 1-fluoro-4-(2-isocyanoethyl)(9CI) is utilized in the synthesis of pharmaceuticals and organic compounds, and it may also find applications in materials science and agricultural chemistry. However, due to its potential toxic or hazardous properties, it is crucial to handle this chemical with caution.
Uses
Used in Pharmaceutical Synthesis:
Benzene, 1-fluoro-4-(2-isocyanoethyl)(9CI) is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the creation of new drug molecules with specific therapeutic properties.
Used in Organic Compounds Synthesis:
Benzene, 1-fluoro-4-(2-isocyanoethyl)(9CI) is also utilized in the synthesis of organic compounds, contributing to the development of new chemical entities with potential applications in various industries.
Used in Materials Science:
Benzene, 1-fluoro-4-(2-isocyanoethyl)(9CI) may have potential applications in materials science, where its unique properties can be leveraged to develop new materials with specific characteristics.
Used in Agricultural Chemistry:
In agricultural chemistry, this compound may be used to develop new agrochemicals or enhance the properties of existing ones, contributing to more effective and sustainable agricultural practices.
Check Digit Verification of cas no
The CAS Registry Mumber 244221-04-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,4,2,2 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 244221-04:
(8*2)+(7*4)+(6*4)+(5*2)+(4*2)+(3*1)+(2*0)+(1*4)=93
93 % 10 = 3
So 244221-04-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H8FN/c1-11-7-6-8-2-4-9(10)5-3-8/h2-5H,6-7H2
244221-04-3Relevant articles and documents
Extended Multicomponent Reactions with Indole Aldehydes: Access to Unprecedented Polyheterocyclic Scaffolds, Ligands of the Aryl Hydrocarbon Receptor
Ghashghaei, Ouldouz,Pedrola, Marina,Seghetti, Francesca,Martin, Victor V.,Zavarce, Ricardo,Babiak, Michal,Novacek, Jiri,Hartung, Frederick,Rolfes, Katharina M.,Haarmann-Stemmann, Thomas,Lavilla, Rodolfo
, p. 2603 - 2608 (2021)
The participation of reactants undergoing a polarity inversion along a multicomponent reaction allows the continuation of the transformation with productive domino processes. Thus, indole aldehydes in Groebke–Blackburn–Bienaymé reactions lead to an initial adduct which spontaneously triggers a series of events leading to the discovery of novel reaction pathways together with direct access to a variety of linked, fused, and bridged polyheterocyclic scaffolds. Indole 3- and 4-carbaldehydes with suitable isocyanides and aminoazines afford fused adducts through oxidative Pictet–Spengler processes, whereas indole 2-carbaldehyde yields linked indolocarbazoles under mild conditions, and a bridged macrocycle at high temperature. These novel structures are potent activators of the human aryl hydrocarbon receptor signaling pathway.
