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N-Hydroxy-2-Methyl-5-[(5-Methyl-2-phenyl-4-oxazolyl)Methyl]-1,3-dioxane-2-carboxaMide

Base Information Edit
  • Chemical Name:N-Hydroxy-2-Methyl-5-[(5-Methyl-2-phenyl-4-oxazolyl)Methyl]-1,3-dioxane-2-carboxaMide
  • CAS No.:1297530-08-5
  • Molecular Formula:C17H20N2O5
  • Molecular Weight:332.356
  • Hs Code.:
  • Mol file:1297530-08-5.mol
N-Hydroxy-2-Methyl-5-[(5-Methyl-2-phenyl-4-oxazolyl)Methyl]-1,3-dioxane-2-carboxaMide

Synonyms:N-(hydroxy)-2-methyl-5-((5-methyl-2-phenyloxazol-4-yl)methyl)-1,3-dioxane-2-carboxamide

Suppliers and Price of N-Hydroxy-2-Methyl-5-[(5-Methyl-2-phenyl-4-oxazolyl)Methyl]-1,3-dioxane-2-carboxaMide
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
  • TRC
  • N-Hydroxy-2-methyl-5-[(5-methyl-2-phenyl-4-oxazolyl)methyl]-1,3-dioxane-2-carboxamide
  • 50mg
  • $ 1320.00
  • Medical Isotopes, Inc.
  • N-Hydroxy-2-methyl-5-[(5-methyl-2-phenyl-4-oxazolyl)methyl]-1,3-dioxane-2-carboxamide
  • 5 mg
  • $ 650.00
Total 2 raw suppliers
Chemical Property of N-Hydroxy-2-Methyl-5-[(5-Methyl-2-phenyl-4-oxazolyl)Methyl]-1,3-dioxane-2-carboxaMide Edit
Chemical Property:
Purity/Quality:

99% *data from raw suppliers

N-Hydroxy-2-methyl-5-[(5-methyl-2-phenyl-4-oxazolyl)methyl]-1,3-dioxane-2-carboxamide *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses N-Hydroxy-2-methyl-5-[(5-methyl-2-phenyl-4-oxazolyl)methyl]-1,3-dioxane-2-carboxamide is a 1,3-dioxane derivative used as PCSK9 inhibitors and is potentially used for the treatment of dyslipidemia and related diseases.
Technology Process of N-Hydroxy-2-Methyl-5-[(5-Methyl-2-phenyl-4-oxazolyl)Methyl]-1,3-dioxane-2-carboxaMide

There total 6 articles about N-Hydroxy-2-Methyl-5-[(5-Methyl-2-phenyl-4-oxazolyl)Methyl]-1,3-dioxane-2-carboxaMide 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:
Multi-step reaction with 2 steps
1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol; N-ethylmorpholine; / N,N-dimethyl-formamide / 5 h / 25 °C / Inert atmosphere
2: ammonium formate / palladium 10% on activated carbon / methanol / Reflux
With N-ethylmorpholine;; ammonium formate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; palladium 10% on activated carbon; In methanol; N,N-dimethyl-formamide;
Guidance literature:
Multi-step reaction with 5 steps
1: ethanol; sodium tetrahydroborate / 6 h / 10 - 25 °C
2: boron trifluoride diethyl etherate / acetonitrile / 18 h / 25 °C / Inert atmosphere
3: water; lithium hydroxide / tetrahydrofuran / 3 h / 20 °C
4: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol; N-ethylmorpholine; / N,N-dimethyl-formamide / 5 h / 25 °C / Inert atmosphere
5: ammonium formate / palladium 10% on activated carbon / methanol / Reflux
With N-ethylmorpholine;; sodium tetrahydroborate; ethanol; boron trifluoride diethyl etherate; water; ammonium formate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; lithium hydroxide; palladium 10% on activated carbon; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; acetonitrile;
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