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Thermo Scientific Chemicals
1,3-Cycloheptanedione, 97%
CAS: 1194-18-9 | C7H10O2 | 126.155 g/mol
| 製品番号（カタログ番号） | 数量 |
|---|---|
| H54588.03 または、製品番号H54588-03 | 1 g |
化学物質識別子
CAS1194-18-9
IUPAC Namecycloheptane-1,3-dione
Molecular FormulaC7H10O2
InChI KeyDBOVMTXPZWVYAQ-UHFFFAOYSA-N
SMILESO=C1CCCCC(=O)C1
さらに表示
仕様
スペックシート
スペックシートAssay (GC)>96.0%
1,3-Cyclopentanedione was used in the synthesis of chemical probes for selective labeling of sulfuric acid proteins. is a versatile reagent for synthesis of perhydroazulenes, prostaglandin products (biologically active unsaturated 20-carbon fatty acids including a 5-carbon ring, derived enzymatically ), and Knoevenagel products.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
1,3-Cyclopentanedione was used in the synthesis of chemical probes for selective labeling of sulfuric acid proteins. is a versatile reagent for synthesis of perhydroazulenes, prostaglandin products (biologically active unsaturated 2
1,3-Cyclopentanedione was used in the synthesis of chemical probes for selective labeling of sulfuric acid proteins. is a versatile reagent for synthesis of perhydroazulenes, prostaglandin products (biologically active unsaturated 2
RUO – Research Use Only
General References:
- Amos B. SmithIII.; Bruce D. Dorsey.; Masashi Ohba.; Andrew T. LupoJr.; Michael S. Malamas. Preparation, reactivity, and spectral properties of 1,3-dioxin vinylogous esters: versatile .beta.-ketovinyl cation equivalents. J. Org. Chem. 1988, 53 (18),4314-4325.
- Hideaki Watanabe , Mitsuhiro Iwamoto.; Masahisa Nakada. Preparation of New Chiral Building Blocks: Highly Enantioselective Reduction of Prochiral 1,3-Cycloalkanediones Possessing a Methyl Group and a Protected Hydroxymethyl Group at Their C2 Position with Baker's Yeast or CBS Catalyst.J. Org. Chem. 2005, 70 (12),4652-4658.