203580-74-9

Basic information

• Product Name: ethyl 2-[(3-methoxyphenyl)-N-methylamino]acetate
• Synonyms: ethyl 2-[(3-methoxyphenyl)-N-methylamino]acetate
• CAS NO: 203580-74-9
• Molecular Weight: 223.272
• Mol File: 203580-74-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: ethyl 2-[(3-methoxyphenyl)-N-methylamino]acetate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2-[(3-methoxyphenyl)-N-methylamino]acetate(203580-74-9)
• EPA Substance Registry System: ethyl 2-[(3-methoxyphenyl)-N-methylamino]acetate(203580-74-9)

Safety Data

• Hazardous Substances Data: 203580-74-9(Hazardous Substances Data)

Upstream product

• 90-04-0 2-methoxy-phenylamine 
• 14318-66-2 3-methoxy-N-methylaniline 
• 105-36-2 ethyl bromoacetate 
• 1314931-05-9 C₈H₉NO 
• 536-90-3 m-Anisidine 

Downstream Products

• 1259926-24-3 pivalic acid 2-[(3-methoxyphenyl)-N-methylamino]ethyl ester 
• 1259926-25-4 pivalic acid 2-[(4-formyl-3-methoxyphenyl)-N-methylamino]ethyl ester 
• 1259926-26-5 pivalic acid 2-{[3-methoxy-4-(2-thiophen-2-ylvinyl)phenyl]-N-methylamino}ethyl ester 
• 33905-43-0 2-[(3-methoxyphenyl)-N-methylamino]ethanol 
• 1259926-29-8 5-(2-{4-[(2-hydroxyethyl) methylamino]-2-methoxyphenyl}vinyl)thiophene-2-carbaldehyde 
• 1259926-28-7 5-[2-(4-{[2-(tert-butylldimethylsilanyloxy)ethyl]methylamino}-2-methoxyphenyl)vinyl]thiophene-2-carbaldehyde 
• 1259926-30-1 2-(3-cyano-4-{2-[5-(2-{4-[(2-hydroxyethyl)methylamino]-2-methoxyphenyl}vinyl)thiophene-2-yl]vinyl}-5-phenyl-5-trifluoromethyl-5H-furan-2-ylidene)malononitrile 

Relevant articles and documents

Fused imidazole compounds with indoleamine 2,3-dioxygenase inhibition activity

The invention relates to fused imidazole compounds, and a preparation method and application thereof. The structure of the compounds is shown in a general formula I, wherein the definitions of each group are as described in the specification. The compounds are capable of selectively inhibiting indoleamine 2,3-dioxygenase (IDO). The compounds provided by the invention can be used as IDO inhibitorsfor the treatment and/or prevention of diseases with the pathological characteristics of IDO mediated tryptophan metabolism pathways, such as cancer, eye diseases, autoimmune diseases, psychological disorders, depression, anxiety and other diseases.

Nonlinear optical side-chain polymers post-functionalized with high-β chromophores exhibiting large electro-optic property

Electro-optic side-chain polymers have been synthesized by the post-functionalization of methacrylate isocyanate polymers with novel phenyl vinylene thiophene vinylene bridge (FTC) nonlinear optical chromophores. For this application, FTC-based chromophores were modified in their electronic donor structure, exhibiting much larger molecular hyperpolarizabilities compared with the benchmark FTC. Of these new chromophores, absorption spectra, hyper-Rayleigh scattering experiment, and thermal analysis were carried out to confirm availability as effective nonlinear optical units for electro-optic side-chain polymers. The electro-optic coefficients (r33) of obtained polymers were investigated in the process of in situ poling by monitoring the temperature, current flow, poling field, and electro-optic signal. Compared with the nonsubstituted analogue, benxyloxy modified FTC chromophore significantly achieved higher nonlinear optical property, exhibiting molecular hyperpolarizability at 1.9 μm of 4600 × 10-30 esu and an r33 value of 150 pm/V at the wavelength of 1.31 μm. Synthesized electro-optic polymers showed high glass transition temperature (Tg), so that the temporal stability examination exhibited >78% of the electro-optic intensity remaining at 85 °C over 500 h. Copyright