177164
1,3-Cyclopentanedione
97%
Synonym(s):
1,3-Cyclopentadione
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About This Item
Linear Formula:
C5H6(=O)2
CAS Number:
Molecular Weight:
98.10
Beilstein/REAXYS Number:
1362728
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
assay
97%
form
powder
mp
149-151 °C (lit.)
storage temp.
2-8°C
SMILES string
O=C1CCC(=O)C1
InChI
1S/C5H6O2/c6-4-1-2-5(7)3-4/h1-3H2
InChI key
LOGSONSNCYTHPS-UHFFFAOYSA-N
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Application
1,3-Cyclopentanedione was used in the synthesis of chemical probes for selective labeling of sulfenic acid proteins.
Versatile reagent for synthesis of perhydroazulenes, PGB1 analogues, and Knoevenagel products.
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Certificates of Analysis (COA)
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The Journal of Organic Chemistry, 58, 3953-3953 (1993)
Aldrichimica Acta, 10, 19-19 (1977)
Synlett, 539-539 (1993)
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
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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
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