422517
2,4,6-三甲氧基嘧啶
99%
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关于此项目
经验公式（希尔记法）:
C7H10N2O3
化学文摘社编号:
分子量:
170.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
产品名称
2,4,6-三甲氧基嘧啶, 99%
InChI
1S/C7H10N2O3/c1-10-5-4-6(11-2)9-7(8-5)12-3/h4H,1-3H3
SMILES string
COc1cc(OC)nc(OC)n1
InChI key
RJVAFLZWVUIBOU-UHFFFAOYSA-N
assay
99%
mp
51-54 °C (lit.)
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.
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.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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