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852597

Sigma-Aldrich

5-Iodouridine

95%

Synonym(s):

2,4-Dihydroxy-5-iodo-1-β-D-ribofuranosylpyrimidine

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About This Item

Empirical Formula (Hill Notation):
C9H11IN2O6
CAS Number:
1024-99-3
Molecular Weight:
370.10
Beilstein/REAXYS Number:
33665
EC Number:
213-833-1
MDL number:
MFCD00006532
UNSPSC Code:
12352100
PubChem Substance ID:
24888326
NACRES:
NA.22

Quality Level

200

assay

95%

form

powder

mp

205-207 °C (dec.) (lit.)

functional group

ether
hydroxyl
iodo

storage temp.

2-8°C

SMILES string

OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N2C=C(I)C(=O)NC2=O

InChI

1S/C9H11IN2O6/c10-3-1-12(9(17)11-7(3)16)8-6(15)5(14)4(2-13)18-8/h1,4-6,8,13-15H,2H2,(H,11,16,17)/t4-,5-,6-,8-/m1/s1

InChI key

RKSLVDIXBGWPIS-UAKXSSHOSA-N

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Related Categories

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
MKBH1547V
04007EH
09712TD
14922LC
09017AZ

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5-Chloro-2′-deoxyuridine thymidine analog

Sigma-Aldrich

C6891

5-Chloro-2′-deoxyuridine

P Martel et al.
Journal of biomolecular structure & dynamics, 12(2), 401-411 (1994-10-01)
This paper reports on the first coherent neutron scattering measurements ever carried out on the vibrational spectrum of a nucleoside analog. Frequencies up to 3.5 Thz belonging to some half-dozen dispersion curves have been measured in a plane normal to
Dehalogenation reactions in fast atom bombardment mass spectrometry.
S K Sethi et al.
Analytical chemistry, 56(11), 1975-1977 (1984-09-01)
Daniel E Ryan et al.
RNA (New York, N.Y.), 10(8), 1251-1265 (2004-07-24)
Elucidation of the three-dimensional (3D) structures of the two sequential active sites in spliceosomes is essential for understanding the mechanism of premessenger RNA splicing. The mechanism is predicted to be catalyzed by the small nuclear RNA (snRNA) components of spliceosomes.
Y Mikata et al.
Biochemistry, 40(25), 7533-7541 (2001-06-20)
Laser-induced photo-cross-linking was investigated for DNA, modified with cisplatin at specific sites, bound to structure-specific recognition domains of proteins in the high-mobility group (HMG) class. The efficiency of photo-cross-linking depends on the wavelength and power of the laser, the nature
Loïc Ropartz et al.
Chemical communications (Cambridge, England), (15)(15), 1556-1558 (2007-04-05)
Novel transition metal catalysts based on oligonucleotides can be easily obtained by functionalization of 5-iodouridine with phosphine ligands, resulting in good asymmetric induction in palladium catalyzed allylic nucleophilic substitution.
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