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Home  > 4-[[3-(1-Methylethyl)-2-oxo-5-oxazolidinyl]methoxy]benzaldehyde

AX32342

1173203-26-3 | 4-[[3-(1-Methylethyl)-2-oxo-5-oxazolidinyl]methoxy]benzaldehyde

Packsize Purity Availability Price Discounted Price    Quantity
5mg 3 weeks $374.00 $262.00 -   +
25mg 3 weeks $1,157.00 $810.00 -   +
50mg 3 weeks $1,915.00 $1,340.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AX32342
Chemical Name: 4-[[3-(1-Methylethyl)-2-oxo-5-oxazolidinyl]methoxy]benzaldehyde
CAS Number: 1173203-26-3
Molecular Formula: C14H17NO4
Molecular Weight: 263.2891
MDL Number: MFCD27967159
SMILES: O=Cc1ccc(cc1)OCC1CN(C(=O)O1)C(C)C

 

Upstream Synthesis Route
  • 4-[[3-(1-Methylethyl)-2-oxo-5-oxazolidinyl]methoxy]benzaldehyde is a versatile compound that finds wide application in chemical synthesis, particularly in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Due to its unique structure and reactivity, this compound serves as a valuable building block in the synthesis of complex organic molecules.One of the key uses of 4-[[3-(1-Methylethyl)-2-oxo-5-oxazolidinyl]methoxy]benzaldehyde is as a key intermediate in the preparation of various biologically active compounds. Its aldehyde group allows for further functionalization through various reactions, enabling the introduction of different substituents to tailor the properties of the final product.In addition, the oxazolidinyl moiety in this compound imparts stereochemical control in asymmetric synthesis, making it a valuable tool in the production of chiral molecules. This feature is particularly important in the pharmaceutical industry, where the activity and selectivity of drugs often depend on the spatial arrangement of atoms in the molecule.Overall, the application of 4-[[3-(1-Methylethyl)-2-oxo-5-oxazolidinyl]methoxy]benzaldehyde in chemical synthesis showcases its importance as a key reagent for the construction of diverse organic compounds with specific functionalities and stereochemistries. Its versatility and synthetic utility make it an indispensable component in the toolkit of synthetic chemists working across various fields.
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