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Thermo Scientific Chemicals
Ethyl 3-(dimethylamino)acrylate, 99%
CAS: 924-99-2 | C7H13NO2 | 143.186 g/mol
化学物質識別子
CAS924-99-2
IUPAC Nameethyl (2Z)-3-(dimethylamino)prop-2-enoate
Molecular FormulaC7H13NO2
InChI KeyMVUMJYQUKKUOHO-WAYWQWQTSA-N
SMILESCCOC(=O)C=C/N(C)C
さらに表示
仕様
スペックシート
スペックシートAppearance (Color)Clear colorless to yellow
FormLiquid
Assay (GC)≥98.5%
Refractive Index1.5105-1.5135 @ 20?C
Ethyl 3-(dimethylamino)acrylate is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff fields.
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
Ethyl 3-(dimethylamino)acrylate is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff fields.
Solubility
Soluble in water 90 g/L (25°C).
Notes
Store in a cool, dry place in tightly closed container. Incompatible with oxidizing agents.
Ethyl 3-(dimethylamino)acrylate is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff fields.
Solubility
Soluble in water 90 g/L (25°C).
Notes
Store in a cool, dry place in tightly closed container. Incompatible with oxidizing agents.
RUO – Research Use Only
General References:
- Violetta Cecchetti; Oriana Tabarrini; Stefano Sabatini; Hua Miao; Enrica Filipponi; Arnaldo Fravolini. Studies on 6-Aminoquinolones: synthesis and antibacterial evaluation of 6-amino-8-ethyl- and 6-amino-8-methoxyquinolones. Bioorganic & Medicinal Chemistry. 1999, 7 (11), 2465-2471.
- Feng V. Yang; William D. Shipe; Jaime L. Bunda; M. Brad Nolt; David D. Wisnoski; Zhijian Zhao; James C. Barrow; William J. Ray; Lei Ma; Marion Wittmann; Matthew A. Seager; Kenneth A. Koeplinger; George D. Hartman; Craig W. Lindsley. Parallel synthesis of N-biaryl quinolone carboxylic acids as selective M1 positive allosteric modulators. Bioorganic & Medicinal Chemistry Letters. 2010, 20 (2), 531-536.