Cytidine 3'-monophosphate

Base Information

• Chemical Name: Cytidine 3'-monophosphate
• CAS No.: 84-52-6
• Molecular Formula: C9H14N3O8P
• Molecular Weight: 323.199
• Hs Code.: HOSPHATE PRODUCT IDENTIFICATION
• European Community (EC) Number: 201-537-5
• UNII: 6DZL5I6D4D
• DSSTox Substance ID: DTXSID301004260
• Nikkaji Number: J4.895J
• Wikidata: Q27104806
• Metabolomics Workbench ID: 49865
• ChEMBL ID: CHEMBL258728
• Mol file: 84-52-6.mol

Synonyms:2' CMP;2'-CMP;3' CMP;3'-CMP;Acid, Cytidylic;Acids, Cytidylic;CMP;Cytidine Monophosphate;Cytidylic Acid;Cytidylic Acids;Monophosphate, Cytidine

Chemical Property of Cytidine 3'-monophosphate

Chemical Property:

• Appearance/Colour: off-white powder
• Melting Point: 230 °C
• Boiling Point: 693.7 °C at 760 mmHg
• PKA: 0.8, 4.28, 6.0(at 25℃)
• Flash Point: 373.4 °C
• Density: 2.15 g/cm³
• Storage Temp.: −20°C
• XLogP3: -3.8
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 8
• Rotatable Bond Count: 4
• Exact Mass: 323.05185141
• Heavy Atom Count: 21
• Complexity: 531

Purity/Quality:

98% ^*data from raw suppliers

Cytidine 3' ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: C1=CN(C(=O)N=C1N)C2C(C(C(O2)CO)OP(=O)(O)O)O
• Isomeric SMILES: C1=CN(C(=O)N=C1N)[C@H]2[C@@H]([C@@H]([C@H](O2)CO)OP(=O)(O)O)O
• Uses: A metabolite of Cytidine (C998300). A highly specific phosphatase that acts on ADP-ribose 1''-phosphate, a metabolite of tRNA splicing in Saccharomyces cerevisiae.

Technology Process of Cytidine 3'-monophosphate

There total 24 articles about Cytidine 3'-monophosphate 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:

Cytidin-(3',5')-adenosin (2382-66-3) → cytidine 2',3'-cyclic monophosphate (633-90-9) + cytidine 3'-monophosphate (84-52-6) + cytidine-2'-monophosphate (85-94-9,27214-06-8) + adenosine (58-61-7)

Guidance literature:

With deuteriated sodium hydroxide; sodium chloride; In water-d2; at 24.84 ℃; pH=10.85 - 13.60; Further Variations:; pH-values; Kinetics;

DOI:10.1021/jo026545o

Reference yield:

Cytidin-(3',5')-adenosin (2382-66-3) → cytidine 3'-monophosphate (84-52-6) + cytidine-2'-monophosphate (85-94-9,27214-06-8) + adenosine (58-61-7)

Guidance literature:

With dinuclear Cu(II) complex 1; HEPES buffer; water; at 25 ℃; pH=7.5; Further Variations:; Catalysts; pH-values; Kinetics;

DOI:10.1039/a808195f

Reference yield:

Cytidin-(3',5')-adenosin (2382-66-3) → cytidine 3'-monophosphate (84-52-6) + adenosine (58-61-7)

Guidance literature:

With tetramethyl ammoniumhydroxide; tetramethylammonium perchlorate; In dimethyl sulfoxide; at 50 ℃; pH=9.9; Kinetics;

DOI:10.1002/chem.201406526

upstream raw materials:

cytidine 2',3'-cyclic monophosphate

CpG

cytidine-2'-monophosphate

C₄₇H₆₀N₁₈O₃₃P₄

Downstream raw materials:

cytidine 2',3'-cyclic monophosphate

CYTIDINE

uridine

uridine-3'-phosphate

Refernces

• 1、 Wildemann, Dirk,Schiene-Fischer, Cordelia,Aumueller, Tobias,Bachmann, Annett,Kiefhaber, Thomas,Luecke, Christian,Fischer, Gunter. "A nearly isosteric photosensitive amide-backbone substitution allows enzyme activity switching in ribonuclease S". . p. 4910 - 4918. Retrieved 2007.
• 2、 -. "COMPOUNDS FOR IMMUNOPOTENTIATION". Page/Page column 151. . Retrieved 2010/02/15.