898767-04-9 Usage
Uses
Used in Organic Synthesis:
3-CHLORO-1-(2-FLUOROPHENYL)-1-OXOPROPANE is used as a building block in organic synthesis for the creation of various biologically active compounds. Its unique structure allows for the development of new molecules with potential applications in various fields.
Used in Pharmaceutical Research:
In pharmaceutical research, 3-CHLORO-1-(2-FLUOROPHENYL)-1-OXOPROPANE is utilized as a key intermediate in the synthesis of pharmaceuticals. Its properties enable the design and development of new drugs with improved therapeutic effects.
Used in Agrochemical Production:
3-CHLORO-1-(2-FLUOROPHENYL)-1-OXOPROPANE is employed in the production of agrochemicals, where it contributes to the development of effective and environmentally friendly products for agricultural applications.
Used in Specialty Chemicals Industry:
3-CHLORO-1-(2-FLUOROPHENYL)-1-OXOPROPANE is also used in the production of specialty chemicals, where its unique properties are leveraged to create high-value products for specific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 898767-04-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,8,7,6 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 898767-04:
(8*8)+(7*9)+(6*8)+(5*7)+(4*6)+(3*7)+(2*0)+(1*4)=259
259 % 10 = 9
So 898767-04-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H8ClFO/c10-6-5-9(12)7-3-1-2-4-8(7)11/h1-4H,5-6H2
898767-04-9Relevant academic research and scientific papers
ISOXAZOLIDINE DERIVED INHIBITORS OF RECEPTOR INTERACTING PROTEIN KINASE 1 (RIPK 1)
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Page/Page column 88; 89, (2017/07/18)
The present disclosure relates generally to methods and compositions for preventing or arresting cell death and/or inflammation.
SUBSTITUTED FLUOROETHYL UREAS AS ALPHA 2 ADRENERGIC AGENTS
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Page/Page column 22; 23, (2008/12/04)
Therapeutic compounds, and methods, compositions, and medicaments related thereto are disclosed herein.
A Convenient Synthesis of 7-Halo-1-indanones and 8-Halo-1-tetralones
Nguyen, Phong,Corpuz, Evelyn,Heidelbaugh, Todd M.,Chow, Ken,Garst, Michael E.
, p. 10195 - 10198 (2007/10/03)
A regioselective oxidation of N-indan-4-yl-acetamide or N-(5,6,7,8-tetrahydronaphthalen-1-yl)acetamide with potassium permanganate followed by acidic hydrolysis gave 7-aminoindan-1-one or 8-aminotetral-1-one in good yield. The amino ketones were converted to the corresponding 7-haloindanone or the 8-halotetralone. Another method to prepare 7-haloindan-1-ones was completed by a cyclization of 3-chloro-1-(2-halophenyl)propan-1-one under Friedel-Crafts conditions to produce the product in gram quantity.
