Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

MRS 2279

Base Information
  • Chemical Name:MRS 2279
  • CAS No.:367909-40-8
  • Molecular Formula:C13H18ClN5O8P2
  • Molecular Weight:469.715
  • Hs Code.:
  • Mol file:367909-40-8.mol
MRS 2279

Synonyms:

Suppliers and Price of MRS 2279
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
  • MRS2279
  • 1mg
  • $ 355.00
  • Tocris
  • MRS2279 ≥98%(HPLC)
  • 1
  • $ 400.00
  • ChemScene
  • MRS2279
  • 1mg
  • $ 880.00
  • ApexBio Technology
  • MRS2279
  • 1mg
  • $ 581.00
  • American Custom Chemicals Corporation
  • MRS-2279 95.00%
  • 5MG
  • $ 500.42
Total 4 raw suppliers
Chemical Property of MRS 2279
Chemical Property:
  • PSA:208.77000 
  • LogP:1.13270 
  • Storage Temp.:Desiccate at -20°C 
Purity/Quality:

97% *data from raw suppliers

MRS2279 *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses MRS 2279 is a selective P2Y1 antagonist with high affinity and results in modulation of aggregation of blood platelets induced by ADP.
Technology Process of MRS 2279

There total 6 articles about MRS 2279 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 boron trichloride; methoxybenzene; In dichloromethane; at 0 ℃; for 24h;
DOI:10.1021/jm990249v
Guidance literature:
Multi-step reaction with 5 steps
1.1: 64 percent / Ph3P; DEAD / tetrahydrofuran / 12 h / 20 °C
2.1: 88 percent / methanol / 12 h / 20 °C
3.1: 39.6 percent / BCl3 / CH2Cl2 / 0.83 h / -78 °C
4.1: LDA / tetrahydrofuran / 0.25 h / -78 °C
4.2: 35 percent / tetrahydrofuran / -78 - 20 °C
5.1: BCl3; anisole / CH2Cl2 / 24 h / 0 °C
With boron trichloride; methoxybenzene; triphenylphosphine; lithium diisopropyl amide; diethylazodicarboxylate; In tetrahydrofuran; methanol; dichloromethane; 1.1: Substitution / 2.1: Substitution / 3.1: Debenzylation / 4.1: Metallation / 4.2: Phosphorylation / 5.1: Debenzylation;
DOI:10.1021/jm990249v
Guidance literature:
Multi-step reaction with 5 steps
1.1: 64 percent / Ph3P; DEAD / tetrahydrofuran / 12 h / 20 °C
2.1: 88 percent / methanol / 12 h / 20 °C
3.1: 39.6 percent / BCl3 / CH2Cl2 / 0.83 h / -78 °C
4.1: LDA / tetrahydrofuran / 0.25 h / -78 °C
4.2: 35 percent / tetrahydrofuran / -78 - 20 °C
5.1: BCl3; anisole / CH2Cl2 / 24 h / 0 °C
With boron trichloride; methoxybenzene; triphenylphosphine; lithium diisopropyl amide; diethylazodicarboxylate; In tetrahydrofuran; methanol; dichloromethane; 1.1: Substitution / 2.1: Substitution / 3.1: Debenzylation / 4.1: Metallation / 4.2: Phosphorylation / 5.1: Debenzylation;
DOI:10.1021/jm990249v
Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 367909-40-8