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cytidylyl-cytidylyl-adenosine

Base Information
  • Chemical Name:cytidylyl-cytidylyl-adenosine
  • CAS No.:2866-39-9
  • Molecular Formula:C28H37 N11 O18 P2
  • Molecular Weight:877.612
  • Hs Code.:
  • Mol file:2866-39-9.mol
cytidylyl-cytidylyl-adenosine

Synonyms:Cytidine,adenylyl-(5'®3')-cytidylyl-(5'®3')- (8CI)

Suppliers and Price of cytidylyl-cytidylyl-adenosine
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
Total 5 raw suppliers
Chemical Property of cytidylyl-cytidylyl-adenosine
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Boiling Point:1206.8°Cat760mmHg 
  • PKA:1.37±0.50(Predicted) 
  • Flash Point:683.6°C 
  • PSA:451.42000 
  • Density:2.28g/cm3 
  • LogP:-3.03720 
Purity/Quality:

97% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of cytidylyl-cytidylyl-adenosine

There total 4 articles about cytidylyl-cytidylyl-adenosine 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 formic acid; In diethyl ether; at 0 ℃; for 0.5h;
DOI:10.1021/jo00233a015
Guidance literature:
With hydrogenchloride; ammonia; zinc(II) chloride; Yield given. Multistep reaction; 1) pyridine, water, 24h room temperature 2) 5h 50 deg C 3) 18h 20 deg C;
DOI:10.1021/jo01304a042
Guidance literature:
With hydrogenchloride; ammonium hydroxide; Yield given. Multistep reaction; 1.) dioxane, 50 deg C, 24 h, 2.) RT, 12.5 h;
DOI:10.1021/jo00343a007
upstream raw materials:

C82H81Cl2N13O24P2

C99H101Cl2N11O28P2

Downstream raw materials:

anthranilic acid

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