457426
5-Iodo-2,4-dimethoxypyrimidine
98%
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About This Item
Empirical Formula (Hill Notation):
C6H7IN2O2
CAS Number:
Molecular Weight:
266.04
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Assay
98%
mp
71-75 °C (lit.)
λmax
277 nm
SMILES string
COc1ncc(I)c(OC)n1
InChI
1S/C6H7IN2O2/c1-10-5-4(7)3-8-6(9-5)11-2/h3H,1-2H3
InChI key
KNTMOGOYRYYUIE-UHFFFAOYSA-N
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Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Nucleic acid components and their analogues. XLIII. Synthesis of anomeric 5-iodo-2'-deoxyuridines.
Prystas M and Sorm F.
Collection of Czechoslovak Chemical Communications, 29(1), 121-130 (1964)
Synthesis of nucleosides. 9. General synthesis of N-glycosides. I. Synthesis of pyrimidine nucleosides.
Niedballa U and Vorbruggen H.
The Journal of Organic Chemistry, 39(25), 3654-3660 (1974)
Synthesis of 5-(acylethynyl) uracils and their corresponding 2'-deoxyribonucleosides through palladium-catalysed reactions.
Kundu BG and Dasgupta SK.
Journal of the Chemical Society. Perkin Transactions 1, 21, 2657-2663 (1993)
Palladium-catalysed carbomethoxyvinylation and thienylation of 5-iodo (bromo)-2, 4-dimethoxypyrimidine in water.
Basnak I, et al.
Tetrahedron Letters, 38(27), 4869-4872 (1997)
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