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Thymidine

Base Information Edit
  • Chemical Name:Thymidine
  • CAS No.:50-88-4
  • Deprecated CAS:35902-13-7
  • Molecular Formula:C10H14N2O5
  • Molecular Weight:0
  • Hs Code.:
  • European Community (EC) Number:200-070-4
  • UNII:VC2W18DGKR
  • DSSTox Substance ID:DTXSID5023661
  • Nikkaji Number:J4.548I
  • Wikipedia:Thymidine
  • Wikidata:Q422464
  • NCI Thesaurus Code:C880
  • Pharos Ligand ID:ZPLW32L1R1P3
  • Metabolomics Workbench ID:37175
  • ChEMBL ID:CHEMBL52609
  • Mol file:50-88-4.mol
Thymidine

Synonyms:2' Deoxythymidine;2'-Deoxythymidine;Deoxythymidine;Thymidine

Suppliers and Price of Thymidine
Supply Marketing:Edit
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 0 raw suppliers
Chemical Property of Thymidine Edit
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • Density:1.452g/cm3 
  • XLogP3:-1.2
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:2
  • Exact Mass:242.09027155
  • Heavy Atom Count:17
  • Complexity:381
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Chemical Classes:Biological Agents -> Nucleic Acids and Derivatives
  • Canonical SMILES:CC1=CN(C(=O)NC1=O)C2CC(C(O2)CO)O
  • Isomeric SMILES:CC1=CN(C(=O)NC1=O)[C@H]2C[C@@H]([C@H](O2)CO)O
  • Recent ClinicalTrials:Treatment of TK2 Deficiency With Thymidine and Deoxycytidine
  • Recent EU Clinical Trials:A phase III, open-label, randomised multicentre study to evaluate the immunogenicity and safety of a booster dose of GlaxoSmithKline Biologicals’ dTpa-IPV vaccine (Boostrix Polio) compared with Sanofi Pasteur MSD’s dTpa-IPV vaccine (Repevax), when co-administered with GSK Biologicals’ MMR vaccine (Priorix) in 3 and 4-year-old healthy children.
Technology Process of Thymidine

There total 455 articles about Thymidine 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 sodium acetate buffer; PDMase; at 37 ℃; for 0.166667h; Rate constant;
DOI:10.1246/bcsj.56.549
Guidance literature:
Multi-step reaction with 4 steps
1: tetrazole / acetonitrile / 4 h / 20 °C / Inert atmosphere
2: water; iodine / tetrahydrofuran; acetonitrile / 20 °C
3: hydrazinium monoacetate / methanol; dichloromethane / 2.5 h
4: water; sodium chloride / 72 h / 37 °C / pH 7.5 / Sealed tube; HEPES buffer; Enzymatic reaction
With tetrazole; water; iodine; hydrazinium monoacetate; sodium chloride; In tetrahydrofuran; methanol; dichloromethane; acetonitrile;
DOI:10.3390/molecules16010552
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