2',3'-Dideoxyuridine

Suppliers

Names

[ CAS No. ]:
5983-09-5

[ Name ]:
2',3'-Dideoxyuridine

[Synonym ]:
1-[5-(Hydroxymethyl)tetrahydro-2-furanyl]-5-methyl-2,4(1H,3H)-pyrimidinedione
1-[5-(hydroxymethyl)tetrahydrofuran-2-yl]-5-methylpyrimidine-2,4(1H,3H)-dione
1-[(2R,5S)-5-(Hydroxymethyl)tetrahydro-2-furanyl]-2,4(1H,3H)-pyrimidinedione
2,4(1H,3H)-Pyrimidinedione, 1-[(2R,5S)-tetrahydro-5-(hydroxymethyl)-2-furanyl]-
2,4(1H,3H)-Pyrimidinedione, 5-methyl-1-[tetrahydro-5-(hydroxymethyl)-2-furanyl]-
MFCD00013359
1-[(2R,5S)-5-(Hydroxymethyl)tetrahydrofuran-2-yl]pyrimidine-2,4(1H,3H)-dione
1-[(2R,5S)-5-(hydroxymethyl)oxolan-2-yl]pyrimidine-2,4-dione

Chemical & Physical Properties

[ Density]:
1.3±0.1 g/cm3

[ Melting Point ]:
127-129 °C(lit.)

[ Molecular Formula ]:
C9H12N2O4

[ Molecular Weight ]:
212.20

[ Exact Mass ]:
226.095352

[ PSA ]:
84.32000

[ LogP ]:
-0.76

[ Index of Refraction ]:
1.552

[ Storage condition ]:
2~8°C

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
C

[ Risk Phrases ]:
34-36/37

[ Safety Phrases ]:
S22-S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2934999090

Synthetic Route

Precursor & DownStream

Precursor

  • 2',3'-Didehydro-2',3'-dideoxyuridine
  • 2'-deoxyuridine
  • Uridine
  • Zalcitabine
  • 5’-O-Acetyl-2’,3’-dideoxy-2’,3’-didehydro-uridine
  • 2',3'-O-(Methoxymethylene)uridine

DownStream

  • [(2S,5R)-5-(2-aminopurin-9-yl)oxolan-2-yl]methanol
  • 2',3'-Dideoxyadenosine
  • Zalcitabine
  • 2',3'-Dideoxyinosine
  • Uracil
  • (2S)-5α-(6-Fluoro-9H-purine-9-yl)tetrahydrofuran-2α-methanol
  • [(2S,5R)-5-(2,6-dichloropurin-9-yl)oxolan-2-yl]methanol
  • (2S)-5α-(6-Bromo-9H-purine-9-yl)tetrahydro-2α-furanmethanol
  • 2',3'-Dideoxy-5-iodouridine
  • [(2S,5R)-5-purin-9-yloxolan-2-yl]methanol

Customs

[ HS Code ]: 2934999090

[ Summary ]:
2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Abacavir and metabolite pharmacokinetics in HIV-1-infected children and adolescents.

J. Acquir. Immune Defic. Syndr. 51(1) , 54-9, (2009)

Abacavir (ABC) oral clearance, adjusted for body size, is approximately 2 times higher for children than adults with a corresponding difference in dose regimens. However, there are limited data availa...

Potent DNA chain termination activity and selective inhibition of human immunodeficiency virus reverse transcriptase by 2',3'-dideoxyuridine-5'-triphosphate.

Mol. Pharmacol. 37(2) , 157-63, (1990)

2',3'-Dideoxyuridine (ddUrd) exhibits poor if any anti-human immunodeficiency virus (HIV) activity in ATH8 and MT-4 cells. This is in agreement with the failure of ddUrd to be efficiently anabolized i...

Glycosyl-oxycarbonylaminosulfonyl-2',3'-dideoxynucleoside derivatives as lipophilic nucleotide mimics. Synthesis and anti-HIV activity.

Bioorg. Med. Chem. 1(4) , 279-84, (1993)

Several lipophilic-2',3'-dideoxynucleotide analogues have been synthesized and tested against Human Immunodeficiency Virus (HIV). Glycosyl-oxycarbonylaminosulfonyl-analogues of 3'-deoxythymidine and 2...


More Articles


Related Compounds

  • 2',3'-Dideoxyuridinene
  • 5-Iodo-2',3'-dideoxyuridine
  • 5-Ethyl-2',3'-dideoxyuridine
  • 5-bromo-2',3'-dideoxyuridine
  • 5-Chloro-2',3'-dideoxyuridine
  • 3'-azido-2',3'-dideoxyuridine
  • 2-(8-Methyl-2-oxoquinolin-1(2H)-yl)acetic acid
  • 2-(3-hydroxypiperidin-3-yl)-N,N-dimethylacetamide
  • 3-[2-(Morpholin-4-yl)ethyl]azetidin-3-ol
  • 1-(Aminomethyl)-8-methoxynaphthalene
  • N-Methoxy-N-methyl-4-(tritylsulfanyl)butanamide
  • 3-(2-Chlorophenyl)-2,3-dihydro-1H-isoindol-1-one
  • N-methyl-3-(pyridin-4-yl)cyclobutan-1-amine
  • 15-Methoxy-1-pentadecanethiol
  • Methyl 4-chloro-1-methyl-1H-pyrrolo[3,2-c]pyridine-2-carboxylate
  • N-[4-[[(Phenylmethoxy)carbonyl]amino]benzoyl]glycine methyl ester
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.