131695
Pyrimidine
≥98.0%
Sinónimos:
1,3-Diazine, Metadiazine, m-Diazine
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Fórmula empírica (notación de Hill):
C4H4N2
Número CAS:
Peso molecular:
80.09
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39161701
UNSPSC Code:
12352100
EC Number:
206-026-0
MDL number:
Beilstein/REAXYS Number:
103894
Assay:
≥98.0%
Servicio técnico
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Permítanos ayudarleQuality Level
assay
≥98.0%
refractive index
n20/D 1.504 (lit.)
bp
123-124 °C (lit.)
mp
19-22 °C (lit.)
solubility
H2O: soluble, alcohols: soluble, diethyl ether: soluble
density
1.016 g/mL at 25 °C (lit.)
SMILES string
c1cncnc1
InChI
1S/C4H4N2/c1-2-5-4-6-3-1/h1-4H
InChI key
CZPWVGJYEJSRLH-UHFFFAOYSA-N
General description
Pyrimidine is a heterocyclic compound with excellent stability. It is used in manufacture of pharmaceuticals, agrochemicals and dyes.
Application
Pyrimidine was used to assess the extent of pyrimidine/purine asymmetry quantitatively. It was also used to study the photoinduced ion chemistry of the halogenated pyrimidines, a class of prototype radiosensitizing molecules.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Flam. Liq. 3
Clase de almacenamiento
3 - Flammable liquids
wgk
WGK 3
flash_point_f
93.2 °F - closed cup
flash_point_c
34 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Y Vladimir Pabon-Martinez et al.
Scientific reports, 7(1), 11043-11043 (2017-09-10)
The anti-gene strategy is based on sequence-specific recognition of double-strand DNA by triplex forming (TFOs) or DNA strand invading oligonucleotides to modulate gene expression. To be efficient, the oligonucleotides (ONs) should target DNA selectively, with high affinity. Here we combined
Pyrimidine: a review on anticancer activity with key emphasis on SAR
Aastha M et al.
Future Journal of Pharmaceutical Sciences, 7, 123-123 (2021)
Mattea Carmen Castrovilli et al.
Journal of the American Society for Mass Spectrometry, 25(3), 351-367 (2014-01-05)
In the present work, we studied the photoinduced ion chemistry of the halogenated pyrimidines, a class of prototype radiosensitizing molecules, in the energy region 9-15 eV. The work was stimulated by previous studies on inner shell site-selective fragmentation of the