Chemical intermediate

15176-29-1

  • Product Name：5-Ethyl-2’-deoxy uridine; Edoxudine
  • Molecular Formula：C11H16 N2 O5
  • Specifications：99%
  • Molecular Weight：256.258
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Product Details;

CasNo： 15176-29-1

Molecular Formula： C11H16 N2 O5

Factory Sells Best Quality 5-Ethyl-2’-deoxy uridine; Edoxudine 15176-29-1 with USP

  • Molecular Formula:C11H16 N2 O5
  • Molecular Weight:256.258
  • Melting Point:152-153° 
  • Boiling Point:°Cat760mmHg 
  • PKA:9.98(at 25℃) 
  • Flash Point:°C 
  • PSA：104.55000 
  • Density:1.389 g/cm3 
  • LogP:-1.26030 

15176-29-1 Relevant articles

Importance of 3′-hydroxyl group of the nucleosides for the reactivity of thymidine phosphorylase from Escherichia coli

Hatano, Akihiko,Harano, Aiko,Kirihara, Masayuki

, p. 232 - 233 (2006)

Thymidine phosphorylase in phosphate buf...

Synthesis of 5-ethylpyrimidine nucleoside analogs

Takenaka, Keiko,Muraoka, Masako,Tsuji, Tadakazu

, p. 669 - 673 (1997)

This paper describes the synthesis of ac...

Letter: Synthesis of C-5 substituted pyrimidine nucleosides via organopalladium intermediates.

Bergstrom,Ruth

, p. 1587 - 1589 (1976)

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Use of Nucleoside Phosphorylases for the Preparation of Purine and Pyrimidine 2′-Deoxynucleosides

Drenichev, Mikhail S.,Alexeev, Cyril S.,Kurochkin, Nikolay N.,Mikhailov, Sergey N.

, p. 305 - 312 (2018)

Enzymatic transglycosylation – the trans...

One-pot approach to functional nucleosides possessing a fluorescent group using nucleobase-exchange reaction by thymidine phosphorylase

Hatano, Akihiko,Kurosu, Masayuki,Yonaha, Susumu,Okada, Munehiro,Uehara, Sanae

, p. 6900 - 6905 (2013/10/08)

Herein, we describe β-selective coupling...

Continuous flow photochemistry for the rapid and selective synthesis of 2′-deoxy and 2′,3′-dideoxynucleosides

Shen, Bo,Jamison, Timothy F.

, p. 157 - 164 (2013/04/10)

A new photochemical flow reactor has bee...

15176-29-1 Process route

5-(1-azido-2-iodoethyl)-2'-deoxyuridine

5-(1-azido-2-iodoethyl)-2'-deoxyuridine

5-(1-azidoethyl)-2'-deoxyuridine

5-(1-azidoethyl)-2'-deoxyuridine

5-(1-aminoethyl)-2'-deoxyuridine hydrogen iodide

5-(1-aminoethyl)-2'-deoxyuridine hydrogen iodide

edoxudine
15176-29-1

edoxudine

Conditions
Conditions Yield
With hydrogen; palladium on activated charcoal; In ethanol; at 25 ℃; for 5h; under 1810.02 Torr;
38%
7%
9%
2'-deoxy-5-ethynyluridine
61135-33-9

2'-deoxy-5-ethynyluridine

edoxudine
15176-29-1

edoxudine

Conditions
Conditions Yield
With hydrogen; palladium on activated charcoal; In ethanol; for 1h; under 760 Torr;
97%

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