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54-42-2

  • Product Name:Idoxuridine
  • Molecular Formula:C9H11IN2O5
  • Molecular Weight:354.101
  • Appearance:crystalline solid
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Product Details

pd_meltingpoint:194 °C(lit.)

Appearance:crystalline solid

Purity:99%

High quality purity >99% Idoxuridine 54-42-2 for sale

  • Molecular Formula:C9H11IN2O5
  • Molecular Weight:354.101
  • Appearance/Colour:crystalline solid 
  • Melting Point:194 °C(lit.) 
  • Refractive Index:30 ° (C=1, 1mol/L NaOH) 
  • PKA:8.25(at 25℃) 
  • PSA:104.55000 
  • Density:2.148 g/cm3 
  • LogP:-1.21810 

54-42-2 Relevant articles

Synthesis of Phosphoramidite Monomers Equipped with Complementary Bases for Solid-Phase DNA Oligomerization

Romero-Pérez, Sonia,López-Martín, Isabel,Martos-Maldonado, Manuel C.,Somoza, álvaro,González-Rodríguez, David

supporting information, p. 41 - 45 (2020/01/03)

We describe the preparation of two monom...

Thermodynamic Reaction Control of Nucleoside Phosphorolysis

Kaspar, Felix,Giessmann, Robert T.,Neubauer, Peter,Wagner, Anke,Gimpel, Matthias

supporting information, p. 867 - 876 (2020/01/24)

Nucleoside analogs represent a class of ...

Site-specific incorporation of multiple units of functional nucleotides into DNA using a step-wise approach with polymerase and its application to monitoring DNA structural changes

Huy Le, Binh,Nguyen, Van Thang,Seo, Young Jun

supporting information, p. 2158 - 2161 (2019/02/20)

We have developed a new method, a step-w...

Bio-catalytic synthesis of unnatural nucleosides possessing a large functional group such as a fluorescent molecule by purine nucleoside phosphorylase

Hatano, Akihiko,Wakana, Hiroyuki,Terado, Nanae,Kojima, Aoi,Nishioka, Chisato,Iizuka, Yu,Imaizumi, Takuya,Uehara, Sanae

, p. 5122 - 5129 (2019/10/05)

Unnatural nucleosides are attracting int...

54-42-2 Process route

2'-deoxyuridine
951-78-0,63844-76-8

2'-deoxyuridine

5-Iodo-2'-deoxyuridine
54-42-2,162239-35-2

5-Iodo-2'-deoxyuridine

Conditions
Conditions Yield
With iodine; silver nitrate; In methanol; at 40 ℃; for 3h;
100%
With iodine; silver nitrate; In methanol; at 40 ℃; for 3h;
100%
With sodium azide; Iodine monochloride; In acetonitrile; at 25 ℃; for 24h; Product distribution; Mechanism; other uracil nucleosides; other halogenation agents; var. temp. and time;
96%
With sodium azide; Iodine monochloride; In acetonitrile; at 25 ℃; for 24h;
96%
With 1-(2-methoxyethyl)-3-methylimidazolium trifluoroacetate; N-iodo-succinimide; at 60 ℃; for 0.0666667h;
89%
With ammonium cerium (IV) nitrate; 1-ethylene glycol monomethyl ether-3-methylimidazolium methanesulfonate; lithium iodide; at 80 ℃; for 0.166667h;
82%
With ammonium cerium (IV) nitrate; iodine; In acetonitrile; at 50 ℃; for 4h;
81%
With ammonium cerium(IV) nitrate; lithium iodide; In methanol; at 80 ℃;
77%
With Iodine monochloride; In methanol; at 50 ℃; for 1.5h;
76%
With iodine; In acetonitrile; Ambient temperature; electrolysis (Pt electrodes, Ag/Ag+ reference, LiClO4 as supporting electrolyte);
75%
With iodine; silver sulfate; In methanol; for 0.2h; Ambient temperature;
71%
With iodine; nitric acid;
With Iodine monochloride; triethylamine; Yield given. Multistep reaction; 1.) MeOH, 30 min, 2.) 1 h;
With iodic acid;
2'-deoxyuridine
951-78-0,63844-76-8

2'-deoxyuridine

5-iodouracil
696-07-1

5-iodouracil

5-Iodo-2'-deoxyuridine
54-42-2,162239-35-2

5-Iodo-2'-deoxyuridine

uracil
66-22-8,144104-68-7,18324-22-6,27072-01-1,2920-92-5,51953-19-6

uracil

Conditions
Conditions Yield
With thymidine phosphorylase from Escherichia coli (E.C. 2.4.2.4) immobilized on Sepabeads EC-EP; In aq. phosphate buffer; at 20 ℃; for 3h; pH=7.5; Reagent/catalyst; Enzymatic reaction;

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