34172-48-0 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
7-Iodo-9H-fluoren-2-amine is utilized as an intermediate in the synthesis of various organic compounds, particularly in the pharmaceutical and agrochemical sectors. Its presence as a key component in these industries is attributed to its ability to facilitate the creation of new drugs and agrochemicals through its reactivity and structural properties.
Used in Organic Synthesis:
As an intermediate, 7-Iodo-9H-fluoren-2-amine is used for the synthesis of complex organic molecules. Its unique structure and reactivity make it a crucial component in the development of novel organic compounds with potential applications in various fields.
Used in Fluorescent Materials and Sensors:
7-Iodo-9H-fluoren-2-amine is used as a component in the development of fluorescent materials and sensors due to its inherent fluorescence properties. This characteristic allows it to be integrated into systems that require detection or imaging capabilities, enhancing their performance and sensitivity.
Used in Chemical Reactions:
7-Iodo-9H-fluoren-2-amine is employed in reactions involving nucleophilic substitution and transition metal-catalyzed reactions, capitalizing on the reactivity of its iodo group. This makes it a versatile agent in advancing chemical processes and syntheses.
Check Digit Verification of cas no
The CAS Registry Mumber 34172-48-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,1,7 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 34172-48:
(7*3)+(6*4)+(5*1)+(4*7)+(3*2)+(2*4)+(1*8)=100
100 % 10 = 0
So 34172-48-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H10IN/c14-10-1-3-12-8(6-10)5-9-7-11(15)2-4-13(9)12/h1-4,6-7H,5,15H2
34172-48-0Relevant academic research and scientific papers
Lanthanide chelate for new chromophore structure
-
Paragraph 0129, (2017/08/26)
The present application discloses novel lanthanide chelate designs (Formula (I) and Formula (III)) having fluorenyl-, fluorenylethynyl, 9H-carbazolyl-, 9H-carbozolylethynyl-, dibenzothiophenyl-, dibenzothiophenylethynyl-, dibenzofuranyl or dibenzofuranylethynyl pyridine chromophores around an emitting lanthanide ion, e.g. an europium ( 111 ) ion. The three-membered ring chromophores exhibit high molar absorptivity and luminescence with lanthanide ions. The application also discloses a detectable molecule comprising a biospecific binding reactant useful in bioaffinity based binding assay, luminescent lanthanide chelating ligands, as well as a solid support conjugated with the chelates.
