72802-25-6 Usage
Uses
Used in Pharmaceutical Industry:
1-(3-Fluoro-4-nitrophenyl)ethanone is used as a synthetic intermediate for the development of various pharmaceutical compounds. Its unique structure allows for the creation of new molecules with potential therapeutic properties, contributing to the advancement of drug discovery and design.
Used in Agrochemical Industry:
In the agrochemical sector, 1-(3-Fluoro-4-nitrophenyl)ethanone is utilized as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides. Its incorporation into these products can enhance their effectiveness in controlling pests and weeds, thereby improving crop yields and agricultural productivity.
Used in Medicinal Research:
1-(3-Fluoro-4-nitrophenyl)ethanone is employed as a subject of interest in medicinal research due to its potential biological activities. Scientists explore its interactions with biological targets to uncover new avenues for the treatment of various diseases and conditions.
Used in Chemical Research:
1-(3-Fluoro-4-nitrophenyl)ethanone's unique properties make it a valuable subject in chemical research, where it is studied for its reactivity, stability, and potential applications in the synthesis of novel chemical entities. This research can lead to the development of new materials and technologies with diverse applications.
Check Digit Verification of cas no
The CAS Registry Mumber 72802-25-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,8,0 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 72802-25:
(7*7)+(6*2)+(5*8)+(4*0)+(3*2)+(2*2)+(1*5)=116
116 % 10 = 6
So 72802-25-6 is a valid CAS Registry Number.
72802-25-6Relevant academic research and scientific papers
METHODS OF MAKING HIGH ENANTIOSELECTIVE SECONDARY ALCOHOLS
-
Paragraph 0072; 0073, (2020/09/08)
A new process to synthesis of compound OBI-3424 R-form and S-form products is provided. The "R-form" compound OBI-3423 was first synthesized with 48% overall yield from compound OBI-3424-5 by installation of the labile phosphate motif at later stage. The stereo chemistry is established by 5 steps chemo-enzyme combination synthesis to afford 99% optical purity, After then, the "S-form" compound OBI-3424 is prepared with improving overall yield of 54% from compound OBI-3424-5. The stereo chemistry is established by 4 steps combination of chemo-enzyme synthesis with excellent optical purity of 99%.
(R)- AND (S)-1-(3-(3-N,N-DIMETHYLAMINOCARBONYL)PHENOXYL-4-NITROPHENYL)-1-ETHYL-N,N'-BIS (ETHYLENE)PHOSPHORAMIDATE, COMPOSITIONS AND METHODS FOR THEIR USE AND PREPARATION
-
Paragraph 0061-0063, (2017/06/12)
Provided herein are optically active compounds of the formulae (ii); and (III) and pharmaceutical compositions thereof. Also provided herein are processes of making these compounds and resolving the racemic mixture or the enrichment of same with in one of
DNA ALKYLATING AGENTS
-
Paragraph 0077; 0078; 0079; 0088; 0091; 0093; 0094, (2016/09/26)
Provided herein are compounds of formula I: wherein the variables are defined herein, processes of making them, and methods of treating cancer comprising administering such compounds.
