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Idremcinal

Base Information Edit
  • Chemical Name:Idremcinal
  • CAS No.:110480-13-2
  • Molecular Formula:C39H69NO12
  • Molecular Weight:743.976
  • Hs Code.:
  • Mol file:110480-13-2.mol
Idremcinal

Synonyms:6,15-Dioxabicyclo[10.2.1]pentadecane,erythromycin deriv.; EM 574; Idremcinal

Suppliers and Price of Idremcinal
Supply Marketing:Edit
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
  • EM574
  • 250ug
  • $ 342.00
  • TRC
  • EM574
  • 1mg
  • $ 235.00
  • Cayman Chemical
  • EM574
  • 1mg
  • $ 209.00
  • Cayman Chemical
  • EM574
  • 500μg
  • $ 110.00
  • American Custom Chemicals Corporation
  • EM574 95.00%
  • 5MG
  • $ 504.97
  • AK Scientific
  • Idremcinal
  • 1mg
  • $ 382.00
  • Adipogen Life Sciences
  • EM574 ≥95%(HPLC)
  • 250 μg
  • $ 110.00
Total 2 raw suppliers
Chemical Property of Idremcinal Edit
Chemical Property:
  • Vapor Pressure:6.53E-30mmHg at 25°C 
  • Boiling Point:804°Cat760mmHg 
  • Flash Point:440.1°C 
  • PSA:165.84000 
  • Density:1.18g/cm3 
  • LogP:3.67090 
Purity/Quality:

98% *data from raw suppliers

EM574 *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses Gastrointestinal prokinetic (motilin agonist). EM574 is an erythromycin derivative that is a motilin receptor antagonist.
Technology Process of Idremcinal

There total 2 articles about Idremcinal 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 N-ethyl-N,N-diisopropylamine; In methanol; at 50 ℃; for 22h;
DOI:10.1248/cpb.37.2687
Guidance literature:
Multi-step reaction with 2 steps
1: 85 percent / acetic acid / 1 h / Ambient temperature
2: 27 percent / N,N-diisopropylethylamine / methanol / 22 h / 50 °C
With N-ethyl-N,N-diisopropylamine; In methanol; acetic acid;
DOI:10.1248/cpb.37.2687
Refernces Edit
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