Cytidylyl(5'.2')adenosine

Base Information

• Chemical Name: Cytidylyl(5'.2')adenosine
• CAS No.: 10318-62-4
• Molecular Formula: C19H25N8O11P
• Molecular Weight: 572.428
• European Community (EC) Number: 233-700-1
• DSSTox Substance ID: DTXSID001312644
• Nikkaji Number: J236.763G
• Mol file: 10318-62-4.mol

Synonyms:Cytidylyl(5'.2')adenosine;EINECS 233-700-1;10318-62-4;Cytidylyl(5'2')adenosine;2'-O-(5'-Cytidylyl)adenosine;Adenylyl-(2'-->5')-cytidine;DTXSID001312644

Chemical Property of Cytidylyl(5'.2')adenosine

Chemical Property:

• Boiling Point: 993.2°Cat760mmHg
• Flash Point: 554.5°C
• Density: 2.23g/cm³
• XLogP3: -5.2
• Hydrogen Bond Donor Count: 7
• Hydrogen Bond Acceptor Count: 15
• Rotatable Bond Count: 8
• Exact Mass: 572.13804064
• Heavy Atom Count: 39
• Complexity: 1040

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CN(C(=O)N=C1N)C2C(C(C(O2)COP(=O)(O)OC3C(C(OC3N4C=NC5=C(N=CN=C54)N)CO)O)O)O
• Isomeric SMILES: C1=CN(C(=O)N=C1N)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)(O)O[C@@H]3[C@@H]([C@H](O[C@H]3N4C=NC5=C(N=CN=C54)N)CO)O)O)O

Technology Process of Cytidylyl(5'.2')adenosine

There total 3 articles about Cytidylyl(5'.2')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:

Reference yield:

cytidine triphosphate (65-47-4,13191-15-6) + ATP (56-65-5,896506-78-8) → A2'p5'A2'p5'C (97226-64-7) + A2'p5'A2'p5'U (97205-06-6) + uridylyl-(5'->2')-adenosine (10061-10-6) + adenylyl(2'-5')cytidine (10318-62-4)

Guidance literature:

cytidine triphosphate; ATP; With potassium chloride; magnesium chloride; at 37 ℃; pH=8; aq. buffer; Enzymatic reaction;

With shrimp alkaline phosphatase; magnesium chloride; at 37 ℃; for 1h; pH=8; aq. buffer; Enzymatic reaction;

DOI:10.3390/md8020235

Reference yield:

cytidine triphosphate (65-47-4,13191-15-6) + ATP (56-65-5,896506-78-8) → C2'p5'A2'p5'C (1170694-62-8) + A2'p5'A2'p5'C (97226-64-7) + A2'p5'A2'p5'U (97205-06-6) + C2'p5'A2'p5'A (1270047-38-5) + A2'p5'A2'p5'A2'p5'C (1270047-39-6) + uridylyl-(5'->2')-adenosine (10061-10-6) + adenylyl(2'-5')cytidine (10318-62-4) + C2'p5'A (22886-36-8)

Guidance literature:

cytidine triphosphate; ATP; With potassium chloride; magnesium chloride; at 37 ℃; pH=8; aq. buffer; Enzymatic reaction;

With shrimp alkaline phosphatase; magnesium chloride; at 37 ℃; for 1h; pH=8; aq. buffer; Enzymatic reaction;

DOI:10.3390/md8020235

Reference yield:

→ adenylyl(2'-5')cytidine (10318-62-4)

Guidance literature:

With hydrogenchloride;

upstream raw materials:

cytidine triphosphate

ATP

Downstream raw materials:

adenosine monophosphate

adenosine 2'-monophosphate

Refernces