3849-75-0 Usage
Uses
Used in Drug Discovery:
5-fluoro-1H-indol-3-yl acetate is used as a chemical building block for the development of new pharmaceutical compounds. Its unique properties, such as the presence of a fluorine atom and a reactive acetate group, make it a promising candidate for the synthesis of diverse compounds with potential biological activities.
Used in Material Science:
5-fluoro-1H-indol-3-yl acetate is used as a starting material for the synthesis of novel materials with specific properties. Its versatile chemical structure allows for the development of materials with potential applications in various industries, such as electronics, coatings, and adhesives.
Used in Chemical Synthesis:
5-fluoro-1H-indol-3-yl acetate is used as a reactant in various chemical reactions, enabling the synthesis of a wide range of compounds. Its reactive acetate group allows for the formation of esters, amides, and other functional groups, making it a valuable intermediate in organic synthesis.
Used in Research and Development:
5-fluoro-1H-indol-3-yl acetate is used as a research tool for studying the properties and behavior of indole derivatives. Its unique structure and reactivity make it an interesting subject for academic and industrial research, potentially leading to new discoveries and applications in various fields.
Used in Pharmaceutical Industry:
5-fluoro-1H-indol-3-yl acetate is used as a key intermediate in the synthesis of pharmaceutical compounds. Its unique properties and reactivity make it a valuable building block for the development of new drugs with potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 3849-75-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,4 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3849-75:
(6*3)+(5*8)+(4*4)+(3*9)+(2*7)+(1*5)=120
120 % 10 = 0
So 3849-75-0 is a valid CAS Registry Number.
3849-75-0Relevant academic research and scientific papers
An iodine effect in ambipolar organic field-effect transistors based on indigo derivatives
Pitayatanakul, Oratai,Iijima, Kodai,Ashizawa, Minoru,Kawamoto, Tadashi,Matsumoto, Hidetoshi,Mori, Takehiko
supporting information, p. 8612 - 8617 (2015/08/24)
5,5′-Diiodoindigo (4) exhibits excellent ambipolar transistor properties with hole/electron mobilities of μh/μe = 0.42/0.85 cm2 V-1 s-1. The halogen substituted indigos show decreasing tilt angles from F to I in the crystals. In addition, the iodine-iodine interaction provides extraordinarily large interchain interaction. However, the X-ray diffraction suggests that the indigo molecules are arranged approximately perpendicular to the substrate in the thin films, probably due to the extra iodine-iodine interaction. The remarkable performance is ascribed to this characteristic supramolecular interaction.
