30084-90-3 Usage
Description
2-Fluorenecarboxaldehyde is a light yellow powder that is an organic compound belonging to the class of aldehydes. It is characterized by the presence of a fluorene ring with a formyl group attached to the second carbon position. 2-FLUORENECARBOXALDEHYDE is known for its chemical reactivity and is commonly used as a building block in the synthesis of various organic molecules.
Uses
Used in Organic Synthesis:
2-Fluorenecarboxaldehyde is used as a key intermediate in the synthesis of a wide range of organic compounds, including pharmaceuticals, agrochemicals, and specialty chemicals. Its reactivity allows for various chemical reactions, such as condensation, reduction, and oxidation, making it a versatile starting material for the preparation of complex organic molecules.
Used in Fluorene-based Compounds:
2-Fluorenecarboxaldehyde is used as a precursor for the preparation of fluorene-based compounds, such as 2-hydroxyl-methyl-fluorene. These compounds have potential applications in various fields, including materials science, optoelectronics, and medicinal chemistry.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-fluorenecarboxaldehyde is used as a building block for the synthesis of drug candidates with potential therapeutic applications. Its unique structure and reactivity enable the development of novel molecules with improved pharmacological properties.
Used in Materials Science:
2-Fluorenecarboxaldehyde is used in the development of advanced materials, such as organic semiconductors, polymers, and coatings. Its incorporation into these materials can enhance their properties, such as electrical conductivity, thermal stability, and mechanical strength.
Used in Research and Development:
2-Fluorenecarboxaldehyde is utilized in research and development laboratories for the exploration of new chemical reactions and the synthesis of novel organic compounds. Its unique properties make it an attractive target for academic and industrial research efforts.
Check Digit Verification of cas no
The CAS Registry Mumber 30084-90-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,0,8 and 4 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 30084-90:
(7*3)+(6*0)+(5*0)+(4*8)+(3*4)+(2*9)+(1*0)=83
83 % 10 = 3
So 30084-90-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H10O/c15-9-10-5-6-14-12(7-10)8-11-3-1-2-4-13(11)14/h1-7,9H,8H2
30084-90-3Relevant articles and documents
Vilsmeier reagent for formylation in solvent-free conditions using microwaves
Paul,Gupta,Gupta
, p. 1115 - 1118 (2007/10/03)
POCl3-DMF over silica gel has been used for the synthesis of β-chlorovinylaldehydes (1-5), 2-aryl-3-formylindoles (6-8), 2-chloro-3-formylquinolines (9-13) and other aromatic aldehydes (14-20) using solvent-free conditions and microwave irradiation.