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经验公式(希尔记法):
C5H5NO
化学文摘社编号:
分子量:
95.10
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
205-520-3
Beilstein/REAXYS Number:
105757
MDL number:
Assay:
97%
InChI key
UBQKCCHYAOITMY-UHFFFAOYSA-N
InChI
1S/C5H5NO/c7-5-3-1-2-4-6-5/h1-4H,(H,6,7)
SMILES string
Oc1ccccn1
assay
97%
bp
280-281 °C (lit.)
mp
105-107 °C (lit.)
Quality Level
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Application
催化剂,用于由环状碳酸酯类化合物和醇类化合物生成 β-氧丙基碳酸酯类化合物的反应以及聚谷氨酸酯的氨解反应。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Journal of the Chemical Society. Perkin Transactions 1, 1749-1749 (1993)
Polymer, 35, 2443-2443 (1994)
Ali A Abdul-Sater et al.
Journal of immunology (Baltimore, Md. : 1950), 195(1), 210-216 (2015-05-29)
IFNs, which transduce pivotal signals through Stat1 and Stat2, effectively suppress the replication of Legionella pneumophila in primary murine macrophages. Although the ability of IFN-γ to impede L. pneumophila growth is fully dependent on Stat1, IFN-αβ unexpectedly suppresses L. pneumophila
Mettu Ravinder et al.
Bioorganic & medicinal chemistry letters, 22(18), 6010-6015 (2012-08-18)
Twenty-six 2-pyridone derivatives (8a-8z), which are structurally analogous to amrinone and milrinone two important cardiotonic drugs, are synthesized and characterized. The synthesis of 2-pyridone derivatives involves addition, followed by cyclization between Baylis-Hillman acetates (7a-7k) and enamino esters or nitriles (3a-3e).
Borys Ośmiałowski et al.
Journal of molecular modeling, 17(10), 2491-2500 (2011-01-05)
The 2-[1H]-pyridone/2-hydroxypyridine tautomeric pair and its 6-substituted complexes have been studied with the use of DFT(M05) method. The intermolecular interaction energy has been calculated and discussed in the light of secondary interaction concept. The attractive secondary interactions of O/NH and
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