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Home  > Chemistry  > Heterocyclic Building Blocks  > Oxazolidines  > (R)-4-Hydroxymethyl-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

AB55740

108149-63-9 | (R)-4-Hydroxymethyl-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $19.00 $14.00 -   +
250mg 95% in stock $33.00 $23.00 -   +
1g 95% in stock $79.00 $55.00 -   +
5g 95% in stock $201.00 $141.00 -   +
25g 95% in stock $915.00 $641.00 -   +
100g 95% in stock $2,625.00 $1,837.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB55740
Chemical Name: (R)-4-Hydroxymethyl-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester
CAS Number: 108149-63-9
Molecular Formula: C11H21NO4
Molecular Weight: 231.2887
MDL Number: MFCD06202686
SMILES: OC[C@@H]1COC(N1C(=O)OC(C)(C)C)(C)C

 

Computed Properties
Complexity: 270  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Heavy Atom Count: 16  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 3  
XLogP3: 0.8  

 

 

Upstream Synthesis Route
  • The compound (R)-tert-Butyl 4-(hydroxymethyl)-2,2-dimethyloxazolidine-3-carboxylate is a versatile building block in chemical synthesis. Its unique structure containing both an oxazolidine ring and a tert-butyl ester group allows it to participate in a variety of synthetic reactions, making it a valuable reagent in organic chemistry.One common application of (R)-tert-Butyl 4-(hydroxymethyl)-2,2-dimethyloxazolidine-3-carboxylate is in asymmetric synthesis. As a chiral compound, it can serve as a chiral auxiliary or ligand in asymmetric transformations, enabling the selective formation of enantiomerically pure products. This is particularly useful in the pharmaceutical industry where enantiomeric purity is often crucial for drug efficacy and safety.Furthermore, the hydroxymethyl group in the molecule can undergo various functional group transformations, allowing for the introduction of additional chemical functionalities through selective reactions. This flexibility makes (R)-tert-Butyl 4-(hydroxymethyl)-2,2-dimethyloxazolidine-3-carboxylate a valuable tool in the design and synthesis of complex organic molecules for a range of applications in medicine, materials science, and other fields of chemistry.
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