16994-13-1

Usage

Uses

Used in Pharmaceutical Industry:
1-(5-Amino-2-nitro-phenyl)-ethanone is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure, which includes both an amino and a nitro group, allows for the development of a wide range of medicinal compounds.
Used in Dye Industry:
In the dye industry, 1-(5-Amino-2-nitro-phenyl)-ethanone is used as a starting material for the production of different types of dyes. Its chemical properties make it suitable for creating a variety of colorants used in various applications.
Used in Research and Development:
1-(5-Amino-2-nitro-phenyl)-ethanone is also utilized in the research and development of new drugs. Its potential biological activities and reactivity make it a valuable compound for exploring novel therapeutic agents and drug candidates.
It is important to reiterate that due to the potential toxicity of 1-(5-Amino-2-nitro-phenyl)-ethanone, proper safety measures should be taken when handling and using 1-(5-AMino-2-nitro-phenyl)-ethanone in any application.

Upstream product

• 56915-87-8 3-trifluoroacetamidoacetophenone 
• 99-03-6 1-(3-aminophenyl)ethanone 
• 7463-31-2 3-Acetamidoacetophenone 
• 6637-18-9 5-acetamido-2-nitroacetophenone 

Downstream Products

• 18640-60-3 5-chloro-2-nitroacetophenone 
• 497863-57-7 C₁₈H₂₄N₂O₇ 
• 497863-58-8 C₂₂H₂₉FN₂O₈ 
• 41877-24-1 1-(5-bromo-2-nitrophenyl)ethane-1-one 
• 56079-07-3 3-acetyl-4-aminobenzonitrile 
• 61955-14-4 5-Azido-2-nitroacetophenon 
• 180343-61-7 2-nitro-5-cyanoacetophenone 

Relevant academic research and scientific papers

Compound used as RET kinase inhibitor and application thereof

The invention relates to a compound used as an RET kinase inhibitor and application thereof, wherein the compound has a structure as shown in a formula F, has good inhibition capability on RET kinase, and has good pharmacodynamic and pharmacokinetic performance and lower toxic and side effects.

Photolabile compound and substrate for oligomer probe array with the same

Provided is a substrate for an oligomer probe array to which a photolabile material having an acetylene derivative is directly attached or attached via a linker.

Photolabile compound, oligomer probe array and substrate for oligomer probe array containing the same, and manufacturing method of the same

A photolabile compound, an oligomer probe array, and a susbtrate for oligomer probe array comprising the same, and a manufacturing method of the same are disclosed. wherein, X is or R1 is hydrogen, an alkyl group, or an acetyl group, R2 is hydrogen, methyl, ethyl, propyl, or phenyl.

Site-specific labelling of caged ATP with deuterium or 18oxygen

[3-D]2-Nitroacetophenone and [alcohol-18O]-1-(2-nitrophenyl)ethyl alcohol were prepared and used to synthesise labelled P3-1-(2-nitrophenyl)ethyl esters of ATP ('caged ATP') with isotope present either as deuterium on the 3-position of the nitrosubstituted ring or as 18oxygen in the bridging position between the terminal phosphate and the nitrophenylethyl group. The availability of the deuterated compounds enabled complete assignment of their 1H NMR spectra.