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2-[3-Amino-4-(2-methylpropoxy)phenyl]-4-methyl-5-thiazolecarboxylic acid ethyl ester

Base Information
  • Chemical Name:2-[3-Amino-4-(2-methylpropoxy)phenyl]-4-methyl-5-thiazolecarboxylic acid ethyl ester
  • CAS No.:144060-92-4
  • Molecular Formula:C17H22 N2 O3 S
  • Molecular Weight:334.43
  • Hs Code.:
  • DSSTox Substance ID:DTXSID40601535
  • Nikkaji Number:J3.610.254C
  • Wikidata:Q72439376
  • Mol file:144060-92-4.mol
2-[3-Amino-4-(2-methylpropoxy)phenyl]-4-methyl-5-thiazolecarboxylic acid ethyl ester

Synonyms:144060-92-4;2-[3-AMINO-4-(2-METHYLPROPOXY)PHENYL]-4-METHYL-5-THIAZOLECARBOXYLIC ACID ETHYL ESTER;ethyl 2-[3-amino-4-(2-methylpropoxy)phenyl]-4-methyl-1,3-thiazole-5-carboxylate;2-[3-Amino-4-(2-methylpropoxy)phenyl]-4-methyl-5-thiazolecarboxylicacid ethylester;RQDZYELGFUZPQX-UHFFFAOYSA-N;SCHEMBL469542;DTXSID40601535;AKOS015900020;AC-9023;Ethyl 2-(3-amino-4-isobutyloxyphenyl)-4-methyl-5-thiazolecarboxylate

Suppliers and Price of 2-[3-Amino-4-(2-methylpropoxy)phenyl]-4-methyl-5-thiazolecarboxylic acid ethyl ester
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Biosynth Carbosynth
  • 2-[3-Amino-4-(2-methylpropoxy)phenyl]-4-methyl-5-thiazolecarboxylicacid ethylester
  • 500 mg
  • $ 305.00
  • Biosynth Carbosynth
  • 2-[3-Amino-4-(2-methylpropoxy)phenyl]-4-methyl-5-thiazolecarboxylicacid ethylester
  • 250 mg
  • $ 175.00
  • Biosynth Carbosynth
  • 2-[3-Amino-4-(2-methylpropoxy)phenyl]-4-methyl-5-thiazolecarboxylicacid ethylester
  • 100 mg
  • $ 88.00
  • Biosynth Carbosynth
  • 2-[3-Amino-4-(2-methylpropoxy)phenyl]-4-methyl-5-thiazolecarboxylicacid ethylester
  • 50 mg
  • $ 51.00
  • Biosynth Carbosynth
  • 2-[3-Amino-4-(2-methylpropoxy)phenyl]-4-methyl-5-thiazolecarboxylicacid ethylester
  • 1 g
  • $ 528.00
  • AK Scientific
  • 2-[3-Amino-4-(2-methylpropoxy)phenyl]-4-methyl-5-thiazolecarboxylicacidethylester
  • 500mg
  • $ 461.00
Total 8 raw suppliers
Chemical Property of 2-[3-Amino-4-(2-methylpropoxy)phenyl]-4-methyl-5-thiazolecarboxylic acid ethyl ester
Chemical Property:
  • Vapor Pressure:1.11E-09mmHg at 25°C 
  • Refractive Index:1.57 
  • Boiling Point:488.2 °C at 760 mmHg 
  • Flash Point:249 °C 
  • PSA:102.68000 
  • Density:1.176g/cm3 
  • LogP:4.49340 
  • XLogP3:4.2
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:7
  • Exact Mass:334.13511374
  • Heavy Atom Count:23
  • Complexity:394
Purity/Quality:

98% *data from raw suppliers

2-[3-Amino-4-(2-methylpropoxy)phenyl]-4-methyl-5-thiazolecarboxylicacid ethylester *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCOC(=O)C1=C(N=C(S1)C2=CC(=C(C=C2)OCC(C)C)N)C
Technology Process of 2-[3-Amino-4-(2-methylpropoxy)phenyl]-4-methyl-5-thiazolecarboxylic acid ethyl ester

There total 3 articles about 2-[3-Amino-4-(2-methylpropoxy)phenyl]-4-methyl-5-thiazolecarboxylic acid ethyl ester 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:
Guidance literature:
With palladium 10% on activated carbon; hydrogen; In ethanol; at 50 ℃; for 14h;
Guidance literature:
Multi-step reaction with 2 steps
1: palladium dichloride; isobutyric Acid; di-tert-butyl(cyclohexyl)phosphine; potassium hydrogencarbonate; copper(I) bromide / toluene / 14 h / 120 °C / Inert atmosphere
2: palladium 10% on activated carbon; hydrogen / ethanol / 14 h / 50 °C
With di-tert-butyl(cyclohexyl)phosphine; palladium 10% on activated carbon; hydrogen; potassium hydrogencarbonate; isobutyric Acid; copper(I) bromide; palladium dichloride; In ethanol; toluene;
Guidance literature:
Multi-step reaction with 3 steps
1: potassium carbonate / N,N-dimethyl-formamide / 22 h / 110 °C / Inert atmosphere
2: palladium dichloride; isobutyric Acid; di-tert-butyl(cyclohexyl)phosphine; potassium hydrogencarbonate; copper(I) bromide / toluene / 14 h / 120 °C / Inert atmosphere
3: palladium 10% on activated carbon; hydrogen / ethanol / 14 h / 50 °C
With di-tert-butyl(cyclohexyl)phosphine; palladium 10% on activated carbon; hydrogen; potassium carbonate; potassium hydrogencarbonate; isobutyric Acid; copper(I) bromide; palladium dichloride; In ethanol; N,N-dimethyl-formamide; toluene;
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