Glycolaldehyde diethyl acetal, stab. with ca 0.1% sodium carbonate, 98%
Glycolaldehyde diethyl acetal, stab. with ca 0.1% sodium carbonate, 98%
Glycolaldehyde diethyl acetal, stab. with ca 0.1% sodium carbonate, 98%
Thermo Scientific Chemicals

Glycolaldehyde diethyl acetal, stab. with ca 0.1% sodium carbonate, 98%

CAS: 621-63-6 | C6H14O3 | 134.175 g/mol
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Catalog number L06282.09
also known as L06282-09
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Chemical Identifiers
CAS621-63-6
IUPAC Name2,2-diethoxyethan-1-ol
Molecular FormulaC6H14O3
InChI KeyIKKUKDZKIIIKJK-UHFFFAOYSA-N
SMILESCCOC(CO)OCC
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear, colorless
Assay (GC)>97.5%
Refractive Index1.4140-1.4180 @ 20?C
FormLiquid
Glycolaldehyde diethyl acetal is used in the preparation of neooxazolomycin, which is a part of the oxazolomycin family of antibiotics. It is also used in the preparation of pyrimidine based inhibitors of phosphodiesterase 7.

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
Glycolaldehyde diethyl acetal is used in the preparation of neooxazolomycin, which is a part of the oxazolomycin family of antibiotics. It is also used in the preparation of pyrimidine based inhibitors of phosphodiesterase 7.

Solubility
Miscible with water, chloroform and ethyl acetate.

Notes
Store in a cool place. Incompatible with strong oxidizing agents, strong acid and bases.
RUO – Research Use Only

General References:

  1. Pereira, N. A. M.; Pinho e Melo, T. M. V. D. Recent Developments in the Synthesis of Dipyrromethanes. A Review. Org. Prep. Proced. Int. 2014, 46 (3), 183-213.
  2. Cankařová, N.; Krchňák, V. Polymer-supported stereoselective synthesis of benzimidazolinopiperazinones. J. Org. Chem. 2012, 77 (13), 5687-5695.