2006314-49-2 Usage
Uses
Used in Pharmaceutical Industry:
(S)-1-(3-fluoro-4-nitrophenyl)ethan-1-ol is used as an intermediate for the synthesis of various pharmaceuticals due to its ability to participate in a range of chemical reactions. The presence of fluoro and nitro groups in its structure allows for the creation of complex organic compounds, which are essential in the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical sector, (S)-1-(3-fluoro-4-nitrophenyl)ethan-1-ol is utilized as a building block for the development of agrochemicals. Its chemical properties make it suitable for the synthesis of compounds that can be used in the production of pesticides, herbicides, and other agricultural chemicals.
Used in Fine Chemicals Industry:
(S)-1-(3-fluoro-4-nitrophenyl)ethan-1-ol is also employed as an intermediate in the fine chemicals industry. Its unique structure and reactivity contribute to the synthesis of specialty chemicals used in various applications, such as fragrances, dyes, and other high-value products.
Organic Synthesis:
(S)-1-(3-fluoro-4-nitrophenyl)ethan-1-ol is used as a versatile building block in organic synthesis for creating a wide array of complex organic compounds. Its fluoro and nitro groups facilitate various chemical reactions, making it an important compound in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 2006314-49-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 2,0,0,6,3,1 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2006314-49:
(9*2)+(8*0)+(7*0)+(6*6)+(5*3)+(4*1)+(3*4)+(2*4)+(1*9)=102
102 % 10 = 2
So 2006314-49-2 is a valid CAS Registry Number.
2006314-49-2Relevant academic research and scientific papers
METHODS OF MAKING HIGH ENANTIOSELECTIVE SECONDARY ALCOHOLS
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Paragraph 0120-0123, (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
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Paragraph 0101-0102, (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
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, (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.
AZIRIDINE CONTAINING DNA ALKYLATING AGENTS
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Paragraph 0050, (2017/01/09)
Provided herein are compounds of formula (I)-(VI), wherein the variables are defined herein, processes of making them, and methods of treating cancer comprising administering such compounds.
