Methyl 3-(4-aminophenoxy)thiophene-2-carboxylate

Base Information

• Chemical Name: Methyl 3-(4-aminophenoxy)thiophene-2-carboxylate
• CAS No.: 103790-38-1
• Molecular Formula: C12H11 N O3 S
• Molecular Weight: 249.29
• Hs Code.: 2934999090
• DSSTox Substance ID: DTXSID70377110
• Wikidata: Q82166181
• Mol file: 103790-38-1.mol

Synonyms:103790-38-1;methyl 3-(4-aminophenoxy)thiophene-2-carboxylate;methyl 3-(4-aminophenoxy)-2-thiophenecarboxylate;DTXSID70377110;MFCD04117804;AKOS005069984;FT-0680247;2X-0728;J-522082;METHYL3-(4-AMINOPHENOXY)-2-THIOPHENECARBOXYLATE

Chemical Property of Methyl 3-(4-aminophenoxy)thiophene-2-carboxylate

Chemical Property:

• Vapor Pressure: 1.72E-06mmHg at 25°C
• Melting Point: 102-105°C
• Boiling Point: 396.4°Cat760mmHg
• Flash Point: 193.5°C
• PSA: 89.79000
• Density: 1.314g/cm³
• LogP: 3.49040
• Storage Temp.: 2-8°C
• XLogP3: 2.6
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 4
• Exact Mass: 249.04596439
• Heavy Atom Count: 17
• Complexity: 267

Purity/Quality:

97% ^*data from raw suppliers

Methyl 3-(4-aminophenoxy)-2-thiophenecarboxylate >95% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COC(=O)C1=C(C=CS1)OC2=CC=C(C=C2)N

Technology Process of Methyl 3-(4-aminophenoxy)thiophene-2-carboxylate

There total 3 articles about Methyl 3-(4-aminophenoxy)thiophene-2-carboxylate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 90.0%

methyl 3-(4-nitrophenoxy)thiophene-2-carboxylate (103790-37-0) → methyl 3-(4-aminophenoxy)thiophene-2-carboxylate (103790-38-1)

Guidance literature:

With iron; acetic acid; In methanol; for 1.25h; Heating;

Reference yield:

methyl 3-hydroxy-2-thiophenecarboxylate (5118-06-9) → methyl 3-(4-aminophenoxy)thiophene-2-carboxylate (103790-38-1)

Guidance literature:

Multi-step reaction with 2 steps

1: 1.) potassium t-butoxide / 1.) methanol, warming, 2.) DMF, reflux, 3 h

2: 90 percent / iron powder, acetic acid / methanol / 1.25 h / Heating

With potassium tert-butylate; iron; acetic acid; In methanol;

Reference yield:

4-Fluoronitrobenzene (350-46-9,178603-76-4) → methyl 3-(4-aminophenoxy)thiophene-2-carboxylate (103790-38-1)

Guidance literature:

Multi-step reaction with 2 steps

1: 1.) potassium t-butoxide / 1.) methanol, warming, 2.) DMF, reflux, 3 h

2: 90 percent / iron powder, acetic acid / methanol / 1.25 h / Heating

With potassium tert-butylate; iron; acetic acid; In methanol;

upstream raw materials:

methyl 3-(4-nitrophenoxy)thiophene-2-carboxylate

methyl 3-hydroxy-2-thiophenecarboxylate

4-Fluoronitrobenzene

Downstream raw materials:

3-<4-(p-toluenesulphonamido)phenoxy>thiophene-2-carboxylic acid

3-[4-(Toluene-4-sulfonylamino)-phenoxy]-thiophene-2-carboxylic acid methyl ester

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