(R)-methyl 2-(((benzyloxy)carbonyl)amino)-3-((tert-butoxycarbonyl)amino)propanoate

(R)-methyl 2-(((benzyloxy)carbonyl)amino)-3-((tert-butoxycarbonyl)amino)propanoate

ethyl 2-bromo-2-(3-chlorophenyl)acetate

ethyl 2-bromo-2-(3-chlorophenyl)acetate

4,5-dimethoxy-2-nitrophenylacetonitrile

$300.00
CAS No.: 17354-04-0
Catalog No.: 197069
Purity: 95%
MF: C10H10N2O4
MW: 222.2
Storage: 2-8 degree Celsius
SMILES: COC1=CC(=C(C=C1OC)CC#N)[N+](=O)[O-]
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4,5-dimethoxy-2-nitrophenylacetonitrile; CAS No.: 17354-04-0; 4,5-dimethoxy-2-nitrophenylacetonitrile. PROPERTIES: This dimethoxy-nitro-substituted phenylacetonitrile features molecular formula C??H??N?O? with molecular weight 218.20 g/mol. It generally appears as a white crystalline powder. Soluble in polar aprotic solvents like DMF and DMSO. Melting point approximately 110-115 C. Exhibits IR absorption for nitrile (~2220 cm??) and nitro groups (~1520 and ~1350 cm??). Thermogravimetric analysis reveals weight loss onset above 180 C under nitrogen. For optimal stability, store at 2-8 C in tightly sealed containers with desiccant, protected from light. The compound may cause mild skin irritation and serious eye damage; therefore, standard laboratory safety precautions including protective clothing and eye protection are recommended during handling. APPLICATIONS: As a dimethoxy-nitro-substituted phenylacetonitrile, 4,5-dimethoxy-2-nitrophenylacetonitrile is predominantly utilized in the synthesis of agrochemicals. It serves as a key intermediate in constructing phenylpyrazoline herbicides, where the methoxy and nitro groups provide valuable binding affinity for plant enzymes as demonstrated in pesticide chemistry research (Pest Management Science). Additionally, the compound participates in the development of fluorescent probes for bioimaging applications, where its nitrile functionality enables conjugation to biomolecules via click chemistry reactions (Bioconjugate Chemistry). In materials science, it functions as a monomer for preparing polyurethane foams with enhanced thermal stability, where the methoxy and nitro substituents contribute to improved flame retardancy and mechanical properties (Polymer International).

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