131695
Pyrimidine
≥98.0%
Synonyme(s) :
1,3-Diazine, Metadiazine, m-Diazine
Se connecter pour consulter les tarifs organisationnels et contractuels.
Sélectionner une taille de conditionnement
Changer de vue
A propos de cet article
Formule empirique (notation de Hill) :
C4H4N2
Numéro CAS:
Poids moléculaire :
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%
Service technique
Besoin d'aide ? Notre équipe de scientifiques expérimentés est là pour vous.
Laissez-nous vous aiderQuality 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
Classe de stockage
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
Faites votre choix parmi les versions les plus récentes :
Déjà en possession de ce produit ?
Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.
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