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3,4,5-trimethoxy-N-(2-methoxyethyl)-N-(4-phenyl-1,3-thiazol-2-yl)benzamide

Base Information
  • Chemical Name:3,4,5-trimethoxy-N-(2-methoxyethyl)-N-(4-phenyl-1,3-thiazol-2-yl)benzamide
  • CAS No.:461000-66-8
  • Molecular Formula:C22H24N2O5S
  • Molecular Weight:428.509
  • Hs Code.:
  • European Community (EC) Number:809-319-7
  • DSSTox Substance ID:DTXSID701346745
  • Nikkaji Number:J3.275.916E
  • ChEMBL ID:CHEMBL4303488
  • Mol file:461000-66-8.mol
3,4,5-trimethoxy-N-(2-methoxyethyl)-N-(4-phenyl-1,3-thiazol-2-yl)benzamide

Synonyms:(3,4,5-trimethoxy-N-(2-methoxyethyl)-N-(4-phenyl-2-thiazolyl)benzamide;Eact

Suppliers and Price of 3,4,5-trimethoxy-N-(2-methoxyethyl)-N-(4-phenyl-1,3-thiazol-2-yl)benzamide
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
  • Usbiological
  • Eact
  • 1mg
  • $ 375.00
  • Usbiological
  • Eact
  • 10mg
  • $ 446.00
  • TRC
  • Eact
  • 2.5mg
  • $ 220.00
  • Tocris
  • Eact ≥99%(HPLC)
  • 50
  • $ 806.00
  • Tocris
  • Eact ≥99%(HPLC)
  • 10
  • $ 195.00
  • Sigma-Aldrich
  • Eact ≥98% (HPLC)
  • 25mg
  • $ 399.00
  • Sigma-Aldrich
  • Eact ≥98% (HPLC)
  • 5mg
  • $ 101.00
  • Matrix Scientific
  • 3,4,5-Trimethoxy-N-(2-methoxyethyl)-N-(4-phenyl-1,3-thiazol-2-yl)benzamide
  • 100mg
  • $ 990.00
  • ChemScene
  • Eact 98.28%
  • 100mg
  • $ 900.00
  • ChemScene
  • Eact 98.28%
  • 50mg
  • $ 550.00
Total 7 raw suppliers
Chemical Property of 3,4,5-trimethoxy-N-(2-methoxyethyl)-N-(4-phenyl-1,3-thiazol-2-yl)benzamide
Chemical Property:
  • Boiling Point:595.9±60.0 °C(Predicted) 
  • PKA:2.27±0.10(Predicted) 
  • PSA:98.36000 
  • Density:1.237±0.06 g/cm3(Predicted) 
  • LogP:4.12910 
  • Storage Temp.:2-8°C 
  • Solubility.:DMSO: soluble20mg/mL, clear 
  • XLogP3:3.7
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:9
  • Exact Mass:428.14059304
  • Heavy Atom Count:30
  • Complexity:520
Purity/Quality:

97% *data from raw suppliers

Eact *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:Xn 
  • Statements: 22 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:COCCN(C1=NC(=CS1)C2=CC=CC=C2)C(=O)C3=CC(=C(C(=C3)OC)OC)OC
  • Description Eact is an activator of the calcium-activated chloride channel anoctamin 1 (ANO1). It increases chloride currents in FRT cells expressing human ANO1 (EC50 = 3 μM). It is selective for ANO1 over cystic fibrosis transmembrane conductance regulator (CFTR) chloride channels and epithelial sodium channels (ENaCs) in FRT cells at 10 μM. Eact (20 μM) increases the rate of submucosal gland fluid secretion in human bronchi isolated from patients with cystic fibrosis and healthy individuals. It increases production of mitochondrial reactive oxygen species (ROS), reduces the mitochondrial membrane potential, and induces apoptosis in rat lung microvascular endothelial cells (RLMVECs), as well as reduces total cell counts in pulmonary artery endothelial cell populations isolated from patients with idiopathic pulmonary arterial hypertension (IPAH). Eact also activates transient receptor potential vanilloid 1 (TRPV1) in HEK293T cells expressing the mouse receptor (EC50 = 11.6 μM) and induces scratching and licking behaviors in wild-type, but not Trpv1-/-, mice.
  • Uses Eact is a Ca2+ activated chloride channel protein, which may be used for the treatment of diseases and disorders involving this particular channel such as cystic fibrosis, disorders related to salivary gland dysfunction, dry eye syndrome and intestinal hypomotility.
Technology Process of 3,4,5-trimethoxy-N-(2-methoxyethyl)-N-(4-phenyl-1,3-thiazol-2-yl)benzamide

There total 2 articles about 3,4,5-trimethoxy-N-(2-methoxyethyl)-N-(4-phenyl-1,3-thiazol-2-yl)benzamide 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:
N-(2-methoxyethyl)-4-phenyl-2-thiazolamine; With pyridine; In toluene; for 0.0833333h;
3,4,5-Trimethoxybenzoyl chloride; In toluene; for 4.5h; Reflux; Inert atmosphere;
Guidance literature:
Multi-step reaction with 2 steps
1.1: ethanol / 4 h / Inert atmosphere; Reflux
2.1: pyridine / toluene / 0.08 h
2.2: 4.5 h / Reflux; Inert atmosphere
With pyridine; In ethanol; toluene;
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