3094-08-4 Usage
Uses
Used in Organic Synthesis:
1-Ethoxy-4-nitro-2-(trifluoromethyl)benzene is used as a reagent in organic synthesis for its ability to participate in a variety of chemical reactions, facilitating the creation of new compounds with diverse applications.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 1-Ethoxy-4-nitro-2-(trifluoromethyl)benzene is utilized as an intermediate. Its presence in the synthesis process contributes to the development of new drugs, highlighting its importance in medicinal chemistry.
Used in Agrochemical Production:
Similarly, in agrochemicals, 1-Ethoxy-4-nitro-2-(trifluoromethyl)benzene serves as an intermediate, playing a crucial role in the synthesis of compounds designed to protect crops and enhance agricultural productivity.
Used in the Preparation of Functionalized Aromatic Compounds:
1-Ethoxy-4-nitro-2-(trifluoromethyl)benzene is used as a building block for the preparation of functionalized aromatic compounds. Its structural features allow for the creation of molecules with specific properties, useful in various chemical and material applications.
Used as a Starting Material for Complex Molecule Synthesis:
1-Ethoxy-4-nitro-2-(trifluoromethyl)benzene also serves as a starting material for the synthesis of more complex molecules, underlining its significance in advancing chemical research and innovation.
Check Digit Verification of cas no
The CAS Registry Mumber 3094-08-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,9 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3094-08:
(6*3)+(5*0)+(4*9)+(3*4)+(2*0)+(1*8)=74
74 % 10 = 4
So 3094-08-4 is a valid CAS Registry Number.
3094-08-4Relevant academic research and scientific papers
Novel and selective 5-HT(2C/2B) receptor antagonists as potential anxiolytic agents: Synthesis, quantitative structure - Activity relationships, and molecular modeling of substituted 1-(3- pyridylcarbamoyl)indolines
Bromidge, Steven M.,Dabbs, Steven,Davies, David T.,Duckworth, D. Malcolm,Forbes, Ian T.,Ham, Peter,Jones, Graham E.,King, Frank D.,Saunders, Damian V.,Starr, Susannah,Thewlis, Kevin M.,Wyman, Paul A.,Blaney, Frank E.,Naylor, Christopher B.,Bailey, Fiona,Blackburn, Thomas P.,Holland, Vicky,Kennett, Guy A.,Riley, Graham J.,Wood, Martyn D.
, p. 1598 - 1612 (2007/10/03)
The synthesis, biological activity, and molecular modeling of a novel series of substituted 1-(3-pyridylcarbamoyl)indolines are reported. These compounds are isosteres of the previously published indole urea 1 (SB- 206553) and illustrate the use of aromatic disubstitution as a replacement for fused five-membered rings in the context of 5-HT(2C/2B) receptor antagonists. By targeting a region of space previously identified as sterically allowed at the 5-HT(2C) receptor but disallowed at the 5-HT(2A) receptor, we have identified a number of compounds which are the most potent and selective 5-HT(2C/2B) receptor antagonists yet reported. 46 (SB-221284) was selected on the basis of its overall biological profile for further evaluation as a novel, potential nonsedating anxiolytic agent. A CoMFA analysis of these compounds produced a model with good predictive value and in addition good qualitative agreement with both our 5-HT(2C) receptor model and our proposed binding mode for this class of ligands within that model.
