tert-Butyl hydrogen malonate, 96%
tert-Butyl hydrogen malonate, 96%
tert-Butyl hydrogen malonate, 96%
tert-Butyl hydrogen malonate, 96%
Thermo Scientific Chemicals

tert-Butyl hydrogen malonate, 96%

CAS: 40052-13-9 | C7H12O4 | 160.169 g/mol
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5 g
25 g
Catalog number H26223.14
also known as H26223-14
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Quantity:
25 g
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Price (EUR)
191,00
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Chemical Identifiers
CAS40052-13-9
IUPAC Name3-(tert-butoxy)-3-oxopropanoic acid
Molecular FormulaC7H12O4
InChI KeyNGGGZUAEOKRHMA-UHFFFAOYSA-N
SMILESCC(C)(C)OC(=O)CC(O)=O
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless to yellow
FormLiquid
Assay (Aqueous acid-base Titration)≥95.0 to ≤105.0%
Assay (Silylated GC)≥95.0%
Identification (FTIR)Conforms
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tert-Butyl hydrogen malonate may be used in the preparation of dendritic precursor to asymmetric methanofullerenes, hapten-3,6-(O,S-dimethylthiophosphoramido)-6-oxohexanoic acid, hapten-4,3-(O,S-dimethylthiophosphoramido)-3-oxopropanoic acid.

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 hydrogen malonate may be used in the preparation of dendritic precursor to asymmetric methanofullerenes, hapten-3,6-(O,S-dimethylthiophosphoramido)-6-oxohexanoic acid, hapten-4,3-(O,S-dimethylthiophosphoramido)-3-oxopropanoic acid.

Solubility
Soluble in ethanol.

Notes
Store in a cool, dry condition in a well sealed container.
RUO – Research Use Only

General References:

  1. Jae Koo Lee; Ki Chang Ahn; Donald W Stoutamire; Shirley J Gee; Bruce D Hammock. Development of an enzyme-linked immunosorbent assay for the detection of the organophosphorus insecticide acephate. Journal of Agricultural and Food Chemistry. 2003, 51 (13), 3695-3703.
  2. Helen S Toogood; Edward J Hollingsworth; Rob C Brown; Ian N Taylor; Stephen J C Taylor; Ray McCague; Jennifer A Littlechild. A thermostable L-aminoacylase from Thermococcus litoralis: cloning, overexpression, characterization, and applications in biotransformations. The Journal of Chemical Thermodynamics. 2002, 6 (2), 111-122.