15258-01-2 Usage
Description
(2-Chloroethyl)-4-fluorobenzamide, a chemical compound with the molecular formula C9H8ClFNO, is a derivative of benzamide that features a chloroethyl group and a fluorine atom attached to the benzene ring. (2-CHLOROETHYL)-4-FLUOROBENZAMIDE holds potential in medicinal chemistry and drug development due to its anti-cancer and anti-inflammatory properties, with the chloroethyl group enhancing its utility in the synthesis of other bioactive compounds.
Uses
Used in Pharmaceutical Industry:
(2-Chloroethyl)-4-fluorobenzamide is used as a precursor in the synthesis of bioactive compounds for its potential anti-cancer and anti-inflammatory properties. The presence of the chloroethyl group makes it a valuable building block for creating new pharmaceutical agents.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (2-chloroethyl)-4-fluorobenzamide serves as a subject of study for understanding its anti-cancer and anti-inflammatory mechanisms, which can contribute to the development of novel therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 15258-01-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,2,5 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 15258-01:
(7*1)+(6*5)+(5*2)+(4*5)+(3*8)+(2*0)+(1*1)=92
92 % 10 = 2
So 15258-01-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H9ClFNO/c10-5-6-12-9(13)7-1-3-8(11)4-2-7/h1-4H,5-6H2,(H,12,13)
15258-01-2Relevant articles and documents
N-vinyl amide and preparation method thereof
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Paragraph 0009; 0010; 0011, (2019/12/25)
The invention relates to N-vinyl amide and a preparation method thereof. The preparation method comprises the following concrete steps: in the presence of triethylamine, reacting acyl chloride with 2-chloroethylamine hydrochloride to obtain corresponding N-(2-chloroethyl)amide, treating the N-(2-chloroethyl)amide with lithium diisopropylamide at room temperature, then adding halogenated hydrocarbon, carrying out a stirring reaction at room temperature for 4 hours, removing the solvent, and performing purification to obtain an N-vinyl amide compound. The preparation method of the invention is simple in synthetic route and uses easily-available raw materials; and the prepared N-vinyl amide compound is a good synthetic intermediate, and has potential biological activity and good application value.
STABILITY OLED MATERIALS AND DEVICES WITH IMPROVED STABILITY
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Page/Page column 98, (2010/11/24)
Organic light emitting materials and devices comprising phosphorescent metal complexes comprising ligands comprising aryl or heteroaryl groups substituted at both ortho positions are described. An organic light emitting device, comprising: an anode; a hole transport layer; an organic emissive layer comprising an emissive layer host and an emissive dopant; an electron impeding layer; an electron transport layer; and a cathode disposed, in that order, over a substrate.
