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Dehydro Barnidipine

Base Information
  • Chemical Name:Dehydro Barnidipine
  • CAS No.:172331-68-9
  • Molecular Formula:C27H27N3O6
  • Molecular Weight:489.528
  • Hs Code.:
  • Mol file:172331-68-9.mol
Dehydro Barnidipine

Synonyms:Dehydro Barnidipine;Methyl 2,6-DiMethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic Acid (3S)-1-(PhenylMethyl)-3-pyrrolidinyl Ester

Suppliers and Price of Dehydro Barnidipine
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
  • TRC
  • DehydroBarnidipine
  • 50mg
  • $ 1540.00
  • TRC
  • DehydroBarnidipine
  • 5mg
  • $ 195.00
  • Biosynth Carbosynth
  • Dehydro barnidipine
  • 50 mg
  • $ 1911.00
  • Biosynth Carbosynth
  • Dehydro barnidipine
  • 2 mg
  • $ 174.90
  • Biosynth Carbosynth
  • Dehydro barnidipine
  • 25 mg
  • $ 1051.50
  • Biosynth Carbosynth
  • Dehydro barnidipine
  • 10 mg
  • $ 578.20
  • Biosynth Carbosynth
  • Dehydro barnidipine
  • 5 mg
  • $ 318.00
Total 6 raw suppliers
Chemical Property of Dehydro Barnidipine
Chemical Property:
  • PSA:114.55000 
  • LogP:4.95260 
Purity/Quality:

> 95% *data from raw suppliers

DehydroBarnidipine *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses A metabolite of Barnidipine (B118700) in human plasma.
Technology Process of Dehydro Barnidipine

There total 10 articles about Dehydro Barnidipine 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:
barnidipine; With hydrogenchloride; In water;
In water; at 20 ℃; for 6h;
Guidance literature:
With manganese(IV) oxide; In dichloromethane; at 20 ℃; for 720h; UV-irradiation;
DOI:10.3390/molecules19011344
Guidance literature:
Multi-step reaction with 7 steps
1: ammonium acetate / isopropyl alcohol / 15 h / 20 °C
2: methanol / 2 h / Reflux
3: sodium hydroxide / 1,2-dimethoxyethane / 2 h / 20 °C
4: cinchonine / water; N,N-dimethyl-formamide / 24 h / 20 - 120 °C
5: phosphorus pentachloride / dichloromethane / 1 h / 0 - 2 °C
6: 3 h / -15 °C
7: manganese(IV) oxide / dichloromethane / 720 h / 20 °C / UV-irradiation
With manganese(IV) oxide; phosphorus pentachloride; ammonium acetate; cinchonine; sodium hydroxide; In methanol; 1,2-dimethoxyethane; dichloromethane; water; N,N-dimethyl-formamide; isopropyl alcohol;
DOI:10.3390/molecules19011344
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