123173-60-4 Usage
Uses
Used in Chemical Synthesis:
2,3-difluoro-4-nitro-Phenol is used as a chemical intermediate for the synthesis of various complex organic molecules. Its unique structure allows for further functionalization and modification, making it a valuable building block in the preparation of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Material Science:
In the field of material science, 2,3-difluoro-4-nitro-Phenol is used as a precursor for the development of novel materials with specific properties. Its incorporation into polymers can lead to materials with altered thermal, mechanical, or electronic properties, depending on the desired application.
Used in Analytical Chemistry:
2,3-difluoro-4-nitro-Phenol is used as a reagent or a reference compound in analytical chemistry. Its distinct spectroscopic properties can be utilized for the identification and quantification of other compounds, as well as in the development of new analytical methods.
Used in Research and Development:
2,3-difluoro-4-nitro-Phenol is used as a research compound in academic and industrial laboratories. Its unique structure and reactivity make it an interesting subject for studies in organic chemistry, materials science, and related fields, contributing to the advancement of scientific knowledge and the development of new technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 123173-60-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,1,7 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 123173-60:
(8*1)+(7*2)+(6*3)+(5*1)+(4*7)+(3*3)+(2*6)+(1*0)=94
94 % 10 = 4
So 123173-60-4 is a valid CAS Registry Number.
123173-60-4Relevant articles and documents
Synthesis of fluorinated halonitrobenzenes and halonitrophenols using tetrafluoroethylene and buta-1,3-dienes as starting building blocks
Lipkind, M. B.,Nefedov, O. M.,Volchkov, N. V.
, p. 2156 - 2163 (2022/01/22)
The gas-phase copyrolysis of tetrafluoroethylene with buta-1,3-diene in a flow reactor at 495–505 °C produces 3,3,4,4-tetrafluorocyclohex-1-ene, which selectively converted to 1,2-difluorobenzene or 1-chloro-2,3-difluorobenzene. The latter can be converted to 2-chloro-3,4-difluoronitrobenzene, 2,3,4-trifluoronitrobenzene, 2,3-difluoro-6-nitrophenol, or 2-chloro-3-fluoro-4-nitrophenol via nitration, fluorodechlorination, and hydrolysis reactions.
LRRK2 INHIBITORS
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Page/Page column 138-139, (2013/02/28)
Provided herein are compounds that inhibit or partially inhibit the activity of leucine rich repeat kinases. Also provided herein are methods of treatment of CNS disorders comprising administration of inhibitors of leucine rich repeat kinases.
Method for producing an optically active 1-substituted 2-propanol
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, (2008/06/13)
A method for producing an optically active 1-substituted 2-propanol of the following formula 1, which comprises reacting a hydroxy aromatic compound of the following formula 2 with an optically active propylene oxide in the presence of a catalyst:AOH??Formula 2CH3C*H(OH)CH2OA??Formula 1wherein A is a univalent aromatic group, and C* is an asymmetric carbon atom.
