(R)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)pent-4-ynoic acid

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(S)-1-(3-(dimethylamino)propyl)-1-(4-fluorophenyl)-1,3-dihydroisobenzofuran-5-carbonitrile

(S)-1-(3-(dimethylamino)propyl)-1-(4-fluorophenyl)-1,3-dihydroisobenzofuran-5-carbonitrile

ethyl 3-(2-chlorophenyl)-3-oxopropanoate

$300.00
CAS No.: 19112-35-7
Catalog No.: LT0129
Purity: 95%
MF: C11H11ClO3
MW: 226.659
Storage: 2-8 degree Celsius
SMILES: ClC1=C(C=CC=C1)C(CC(=O)OCC)=O
For R&D use only. Not for human or animal use.
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CAS NO.: 19112-35-7;ethyl 3-(2-chlorophenyl)-3-oxopropanoate. PROPERTIES: This chlorinated ester presents as a colorless liquid with a molecular weight of approximately 222.6 g/mol. The ethyl 3-(2-chlorophenyl)-3-oxopropanoate combines an ethyl ester with a chlorophenyl substituent and a ketone functionality. It exhibits limited aqueous solubility but good dissolution in ethyl acetate and methanol. Stability characterization reveals sensitivity to base-catalyzed hydrolysis of the ester group and light exposure, necessitating storage at 2-8 degree Celsius in amber glass containers. Handlers should use powder hoods with HEPA filtration and wear cut-resistant gloves during handling. Skin contact may cause mild irritation requiring thorough washing. Inhalation may induce respiratory tract irritation; treatment includes fresh air and medical evaluation. Eye exposure requires extended rinsing and possible corticosteroid application. Waste should be hydrolyzed with dilute acid prior to disposal. APPLICATIONS: The ethyl 3-(2-chlorophenyl)-3-oxopropanoate serves as a key intermediate in the synthesis of various pharmaceuticals. Its alpha-keto ester framework provides opportunities for nucleophilic addition reactions. Research teams utilize this compound as a starting material for creating beta-lactam antibiotics and nonsteroidal anti-inflammatory agents. The chlorophenyl group enhances metabolic resistance in resulting drug candidates. Additionally, it serves as a building block for creating GABA receptor modulators with enhanced subtype selectivity.

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