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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
223-372-8
Beilstein/REAXYS Number:
1362728
MDL number:
Product Name
1,3-Cyclopentanedione, 97%
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
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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
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Aldrichimica Acta, 10, 19-19 (1977)
The Journal of Organic Chemistry, 58, 3953-3953 (1993)
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
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
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