3849-75-0 Usage
General Description
5-fluoro-1H-indol-3-yl acetate is a chemical compound with the molecular formula C11H9FNO2. It is a derivative of indole, a heterocyclic compound that is commonly found in natural products and pharmaceuticals. The addition of a fluorine atom to the indole ring imparts unique properties to the compound, potentially making it useful in various applications such as drug discovery and material science. The acetate group attached to the indole ring provides a reactive site for chemical modifications, allowing for the synthesis of diverse compounds with potential biological activities. Overall, 5-fluoro-1H-indol-3-yl acetate is a versatile chemical building block with a wide range of potential uses.
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 articles and documents
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.
