Ibacitabine

Modify Date: 2024-01-03 00:26:36

Ibacitabine Structure
Ibacitabine structure
Common Name Ibacitabine
CAS Number 611-53-0 Molecular Weight 353.114
Density 2.4±0.1 g/cm3 Boiling Point 522.1±60.0 °C at 760 mmHg
Molecular Formula C9H12IN3O4 Melting Point 185 °C
MSDS Chinese USA Flash Point 269.6±32.9 °C
Symbol GHS07
GHS07
Signal Word Warning

 Use of Ibacitabine


Ibacitabine, an antiviral compound, can be used for gene sequencing[1].

 Names

Name 5-Iodo-2'-deoxycytidine
Synonym More Synonyms

 Ibacitabine Biological Activity

Description Ibacitabine, an antiviral compound, can be used for gene sequencing[1].
Related Catalog
References

[1]. A Serpentier-Daude, Contact dermatitis to topical antiviral drugs. Ann Dermatol Venereol. 2000 Feb;127(2):191-3.

 Chemical & Physical Properties

Density 2.4±0.1 g/cm3
Boiling Point 522.1±60.0 °C at 760 mmHg
Melting Point 185 °C
Molecular Formula C9H12IN3O4
Molecular Weight 353.114
Flash Point 269.6±32.9 °C
Exact Mass 352.987244
PSA 110.60000
LogP -0.69
Vapour Pressure 0.0±3.1 mmHg at 25°C
Index of Refraction 1.815
Storage condition Store at 0°C

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H302
Personal Protective Equipment dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes Xn,T
Risk Phrases R22
Safety Phrases 23-26-36/37/39
RIDADR NONH for all modes of transport
HS Code 2934999090

 Synthetic Route

~61%

Ibacitabine Structure

Ibacitabine

CAS#:611-53-0

Literature: Organic Letters, , vol. 12, # 24 p. 5671 - 5673

 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%

 Articles29

More Articles
In vitro sensitivity of macropodid herpesvirus 2 to selected anti-herpetic compounds.

J. Wildl. Dis. 32(1) , 117-20, (1996)

We tested the in vitro sensitivity of Macropodid Herpesvirus 2 to eight commonly used anti-herpetic compounds using plaque reduction tests, March and April, 1995. The virus was most susceptible to inh...

[Antiviral drugs].

Rev. Prat. 35(47) , 2867-71, (1985)

Carbocyclic analogues of 5-halocytosine nucleosides.

J. Med. Chem. 29(9) , 1720-5, (1986)

Carbocyclic analogues of 5-halocytosine nucleosides were prepared by direct halogenation of the carbocyclic analogues of cytidine, 2'-deoxycytidine, 3'-deoxycytidine, or ara-C. The 5-chloro and 5-brom...

 Synonyms

EINECS 210-269-8
MFCD00038063
4-Amino-1-(2-deoxy-β-D-erythro-pentofuranosyl)-5-iodpyrimidin-2(1H)-on
4-Amino-1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)tetrahydro-2-furanyl]-5-iodo-2(1H)-pyrimidinone
Cytidine, 2'-deoxy-5-iodo-
Ibacitabine
2'-Deoxy-5-iodocytidine
4-amino-1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-iodopyrimidin-2-one
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