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About This Item
Empirical Formula (Hill Notation):
C7H10N2O3
CAS Number:
Molecular Weight:
170.17
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
99%
mp
51-54 °C (lit.)
SMILES string
COc1cc(OC)nc(OC)n1
InChI
1S/C7H10N2O3/c1-10-5-4-6(11-2)9-7(8-5)12-3/h4H,1-3H3
InChI key
RJVAFLZWVUIBOU-UHFFFAOYSA-N
General description
2,4,6-Trimethoxypyrimidine is a pyrimidine derivative. One of the methods reported for its synthesis is by the reaction of 2,4,6-trichloropyrimidine with sodium ethoxide at 70-100°C. Its transformation into 1,6-dihydro-2,4-dimethoxy-1-methyl-6-oxopyrimidine by Hilbert-Johnson reaction has been reported.
Application
2,4,6-Trimethoxypyrimidine may be used as a model compound in a study to determine the qualitative composition of mixtures formed during the methylation of barbituric acid and its derivatives by diazomethane.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
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
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Solvation effects in the methylation of barbituric acid and its derivatives by diazomethane.
Krasnov KA, et al.
Chemistry of Heterocyclic Compounds, 23(11), 1218-1221 (1987)
Chemistry of heterocyclic compounds. 29. Synthesis and reactions of multihetero macrocycles possessing 2, 4-pyrimidino subunits connected by carbon-oxygen and/or-sulfur linkages.
Newkome GR, et al.
The Journal of Organic Chemistry, 43(17), 3362-3367 (1978)
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