75476-80-1 Usage
Nitro-substituted derivative
Indene 1H-Indene, 6-nitrois a derivative of indene, which is a bicyclic hydrocarbon molecule, with a nitro group (-NO2) substituting one of its hydrogen atoms.
Applications
Dyes, pharmaceuticals, and agrochemicals 1H-Indene, 6-nitrois commonly used in the production of various dyes, pharmaceuticals, and agrochemicals due to its chemical properties.
Intermediate in synthesis
Organic compounds The compound serves as an intermediate in the synthesis of various organic compounds, making it a useful building block for creating other chemicals and materials.
Nitro group importance
Synthesis building block The presence of the nitro group in 1H-Indene, 6-nitromakes it an important building block for the synthesis of other chemicals and materials, as the nitro group can undergo various chemical reactions.
Potential biological activity
Medicinal uses 1H-Indene, 6-nitrois known to have some potential biological activity, and it is being studied for its possible medicinal applications.
Interest to researchers and industries
Unique chemical structure and diverse applications Due to its unique chemical structure and wide range of applications, 1H-Indene, 6-nitrois of interest to researchers and industries in various fields, including chemistry, pharmaceuticals, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 75476-80-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,4,7 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 75476-80:
(7*7)+(6*5)+(5*4)+(4*7)+(3*6)+(2*8)+(1*0)=161
161 % 10 = 1
So 75476-80-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H7NO2/c11-10(12)9-5-4-7-2-1-3-8(7)6-9/h1-2,4-6H,3H2
75476-80-1Relevant articles and documents
Solvolysis Mechanism of Indan-2-yl Arenesulfonates
Lee, Ikchoon,Lee, Young Sook,Lee, Bon-Su,Lee, Hai Whang
, p. 1441 - 1445 (2007/10/02)
The solvolysis rates of 5-(Y)-substituted indan-2-yl (Z)-benzenesulfonates were determined in a variety of protic solvents at 45.0, 55.0 and 65.0 deg C.Application of an extended Grunwald-Winstein equation indicates that kinetic responses to both solvent ionizing power, YOTs, and solvent nucleophilicity, NOTs, are relatively low but increase in parallel with increasing leaving ability, m = 0.39-0.46 and I=0.32-0.41 for Z=p-Me p-NO2.The magnitude of cross-interaction constant, ρYZ, is also relatively small (0.16-0.32), which is, however, much more dependent on the nucleophilicity rather than the ionizing power of the solvent.These are consistent with the typical SN2 mechanism proceeding through a transition state in which solvent participates in both bond-making and -breaking processes.
