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线性分子式:
C5H6(=O)2
化学文摘社编号:
分子量:
98.10
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
223-372-8
Beilstein/REAXYS Number:
1362728
MDL number:
Assay:
97%
Form:
powder
InChI key
LOGSONSNCYTHPS-UHFFFAOYSA-N
InChI
1S/C5H6O2/c6-4-1-2-5(7)3-4/h1-3H2
SMILES string
O=C1CCC(=O)C1
assay
97%
form
powder
mp
149-151 °C (lit.)
functional group
ketone
storage temp.
2-8°C
Quality Level
Application
1,3-环戊二酮被用于合成化学探针,用于选择性标记亚磺酸蛋白质。
多功能试剂,用于合成全氢薁(perhydroazulene)类物质、PGB1类似物和Knoevenagel反应产物。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Synlett, 539-539 (1993)
The Journal of Organic Chemistry, 58, 3953-3953 (1993)
Carole Reymond et al.
Talanta, 205, 120063-120063 (2019-08-28)
A high number of factors controlled by the experimenter has to be optimized to successfully separate, ionize and detect compounds when analyzing complex matrices by liquid chromatography hyphenated to high resolution mass spectrometry (LC-UV/MS). Key steps to manage such hyphenation
Jiang Qian et al.
Chemical communications (Cambridge, England), 47(32), 9203-9205 (2011-07-09)
Facile, two-step synthesis and kinetic characterization of new chemical probes for selective labeling of sulfenic acid (-SOH) in proteins are presented. The synthesis route relies on the simple and highly efficient Michael addition of thiol containing tags or linkers to
Aldrichimica Acta, 10, 19-19 (1977)
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