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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:
产品名称
1,3-环戊二酮, 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-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)
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
Access to Protected 2-Alkylidene 1,3-diones by Modified Knoevenagel Reaction in the Presence of Thiophenol. A New Approach to Spirocyclopentanol Construction
Klaus Fuchs and Leo A. Paquette
The Journal of Organic Chemistry, 59, 528-528 (1994)
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