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2'-DEOXY-3,4,5,6-TETRAHYDROURIDINE

Base Information Edit
  • Chemical Name:2'-DEOXY-3,4,5,6-TETRAHYDROURIDINE
  • CAS No.:31962-88-6
  • Molecular Formula:C9H16N2O5
  • Molecular Weight:232.236
  • Hs Code.:
  • Mol file:31962-88-6.mol
2'-DEOXY-3,4,5,6-TETRAHYDROURIDINE

Synonyms:2(1H)-Pyrimidinone,1-(2-deoxy-b-D-erythro-pentofuranosyl)tetrahydro-4-hydroxy-(8CI); 2'-Deoxytetrahydrouridine; Tetrahydrodeoxyuridine

Suppliers and Price of 2'-DEOXY-3,4,5,6-TETRAHYDROURIDINE
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
  • American Custom Chemicals Corporation
  • 2'-DEOXY-3,4,5,6-TETRAHYDROURIDINE 95.00%
  • 50MG
  • $ 1904.02
  • American Custom Chemicals Corporation
  • 2'-DEOXY-3,4,5,6-TETRAHYDROURIDINE 95.00%
  • 5MG
  • $ 749.60
Total 8 raw suppliers
Chemical Property of 2'-DEOXY-3,4,5,6-TETRAHYDROURIDINE Edit
Chemical Property:
  • Vapor Pressure:7.55E-18mmHg at 25°C 
  • Boiling Point:617.8°Cat760mmHg 
  • PKA:12.58±0.40(Predicted) 
  • Flash Point:327.4°C 
  • PSA:105.75000 
  • Density:1.488g/cm3 
  • LogP:-2.23380 
Purity/Quality:

97% *data from raw suppliers

2'-DEOXY-3,4,5,6-TETRAHYDROURIDINE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses The novel compound 2'-Deoxy-3,4,5,6-tetrahydrouridine is specifically used to inhibit deaminating enzymes, which would inactivate cytosine arabinoside by conversion to uridine arabinoside. Cytosine arabinoside is used for its anti-viral, particularly anti-herpes and anticytotoxic activity in mammals and birds, as well as to destroy phages which interfere with the production of antibiotics.
Technology Process of 2'-DEOXY-3,4,5,6-TETRAHYDROURIDINE

There total 2 articles about 2'-DEOXY-3,4,5,6-TETRAHYDROURIDINE 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 tetrahydroborate; In water; at 0 ℃; for 2h;
DOI:10.1021/jo802599v
Guidance literature:
With sodium tetrahydroborate;
DOI:10.1021/jo802599v
upstream raw materials:

Tetrahydrodeoxyuridine

Refernces Edit
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