914225-53-9 Usage
Uses
Used in Organic Synthesis:
4-BorMo-3-chloro-5-(trifluoroMethyl)nitrobenzene[2-BroMo-3-chloro-5-nitrobenzotrifluoride] is used as a building block in organic synthesis for its reactivity towards nucleophiles, allowing it to be used in various coupling reactions to form carbon-carbon bonds.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 4-BorMo-3-chloro-5-(trifluoroMethyl)nitrobenzene[2-BroMo-3-chloro-5-nitrobenzotrifluoride] is used as a key intermediate in the synthesis of complex organic molecules with potential therapeutic properties.
Used in Agrochemical Production:
4-BorMo-3-chloro-5-(trifluoroMethyl)nitrobenzene[2-BroMo-3-chloro-5-nitrobenzotrifluoride] is utilized as a precursor in the development of agrochemicals, contributing to the creation of effective compounds for crop protection and enhancement.
Used in Fluorinated Compounds Production:
Due to its trifluoromethyl group, 4-BorMo-3-chloro-5-(trifluoroMethyl)nitrobenzene[2-BroMo-3-chloro-5-nitrobenzotrifluoride] is used as a valuable component in the production of fluorinated compounds, which possess unique properties and are applied in various chemical and material science applications.
Check Digit Verification of cas no
The CAS Registry Mumber 914225-53-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,4,2,2 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 914225-53:
(8*9)+(7*1)+(6*4)+(5*2)+(4*2)+(3*5)+(2*5)+(1*3)=149
149 % 10 = 9
So 914225-53-9 is a valid CAS Registry Number.
914225-53-9Relevant academic research and scientific papers
Synthesis method of 2-(2, 2-difluoroethyoxyl)-6-trifluoromethyl benzenesulfonyl chloride
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Paragraph 0077-0080, (2021/06/13)
The invention discloses a synthesis method of 2-(2, 2-difluoroethyoxyl)-6-trifluoromethyl benzenesulfonyl chloride. The preparation method comprises the following steps: dissolving 2-trifluoromethyl-4-nitro-bromobenzene in sulfuric acid, adding a halogenating reagent, and reacting at 50-100 DEG C for 1-8 hours; dissolving the obtained 2-bromo-3-trifluoromethyl-5-nitro-benzene halide in a solvent, and performing reduction in a reduction system; carrying out diazotization on the obtained 3-halo-4-bromo-5-trifluoromethyl-aniline, and then carrying out decomposition on the obtained 3-halo-4-bromo-5-trifluoromethyl-aniline; carrying out Grignard reaction on the obtained 2-bromo-3-trifluoromethyl-benzene halide, and then reacting with dialkyl disulfide; carrying out etherification reaction on the obtained 2-alkylthio-3-trifluorotoluene-benzene halide and 2, 2-difluoroethanol in an organic solvent under the action of an alkali; and reacting the obtained 2-(2, 2-difluoroethoxy)-6-trifluoromethyl-phenylalkyl sulfide with chlorine gas at 10-60 DEG C for 1-5 hours. The method is short in route, mild in condition, high in yield and suitable for industrial production.
