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Thermo Scientific Chemicals
tert-Butyl ethyl malonate, 95%
CAS: 32864-38-3 | C9H16O4 | 188.223 g/mol
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Catalog number A11927.22
also known as A11927-22
Price (USD)
464.65
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516.00Save 51.35 (10%)
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Quantity:
100 g
Price (USD)
464.65
Online Exclusive
516.00Save 51.35 (10%)
Each
Chemical Identifiers
CAS32864-38-3
IUPAC Name1-tert-butyl 3-ethyl propanedioate
Molecular FormulaC9H16O4
InChI KeyOCOBFMZGRJOSOU-UHFFFAOYSA-N
SMILESCCOC(=O)CC(=O)OC(C)(C)C
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Specifications
Specification Sheet
Specification SheetAppearance (Color)Clear colorless
Refractive Index1.4130-1.4190 @ 20?C
Assay (GC)≥94.0%
FormLiquid
tert-Butyl ethyl malonate is used in the preparation of polar ester-functionalized aliphatic polysulfone. It is also a useful reagent for organic synthesis.
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
tert-Butyl ethyl malonate is used in the preparation of polar ester-functionalized aliphatic polysulfone. It is also a useful reagent for organic synthesis.
Solubility
Miscible with most common solvents. Immiscible with water.
Notes
Incompatible with strong oxidizing agents.
tert-Butyl ethyl malonate is used in the preparation of polar ester-functionalized aliphatic polysulfone. It is also a useful reagent for organic synthesis.
Solubility
Miscible with most common solvents. Immiscible with water.
Notes
Incompatible with strong oxidizing agents.
RUO – Research Use Only
General References:
- Pellissier, H. Recent Developments in Enantioselective Nickel(II)-Catalyzed Conjugate Additions. Adv. Synth. Catal. 2015, 357 (13), 2745-2780.
- Thomas, J. B.; Giddings, A. M.; Olepu, S.; Wiethe, R. W.; Warner, K. R.; Sarret, P.; Longpre, J. M.; Runyon, S. P.; Gilmour, B. P. The amide linker in nonpeptide neurotensin receptor ligands plays a key role in calcium signaling at the neurotensin receptor type 2. Bioorg. Med. Chem. Lett. 2015, 25 (10), 2060-2064.