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Home  > Chemistry  > Heterocyclic Building Blocks  > Oxazolidines  > (S)-1-Boc-2,2-dimethyl-4-hydroxymethyl-oxazolidine

AE12471

108149-65-1 | (S)-1-Boc-2,2-dimethyl-4-hydroxymethyl-oxazolidine

Packsize Purity Availability Price Discounted Price    Quantity
100mg 97% in stock $8.00 $6.00 -   +
250mg 97% in stock $12.00 $9.00 -   +
500mg 97% in stock $20.00 $14.00 -   +
1g 97% in stock $39.00 $27.00 -   +
5g 97% in stock $90.00 $63.00 -   +
10g 97% in stock $161.00 $113.00 -   +
25g 97% in stock $370.00 $259.00 -   +
100g 97% in stock $1,317.00 $922.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AE12471
Chemical Name: (S)-1-Boc-2,2-dimethyl-4-hydroxymethyl-oxazolidine
CAS Number: 108149-65-1
Molecular Formula: C11H21NO4
Molecular Weight: 231.2887
MDL Number: MFCD11041410
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
  • (S)-tert-Butyl 4-(hydroxymethyl)-2,2-dimethyloxazolidine-3-carboxylate is a valuable compound used in chemical synthesis for its versatile applications. This compound serves as a chiral building block in the synthesis of various pharmaceuticals, agrochemicals, and other fine chemicals. Its unique molecular structure, with a protected hydroxymethyl group and a chiral oxazolidine ring, makes it a useful intermediate in the asymmetric synthesis of complex molecules.In organic synthesis, (S)-tert-Butyl 4-(hydroxymethyl)-2,2-dimethyloxazolidine-3-carboxylate can be employed as a key component in the preparation of chiral ligands, catalysts, and intermediates for asymmetric reactions. The chiral nature of this compound allows for the control of stereochemistry in the formation of new chemical entities, enabling chemists to selectively produce enantiopure compounds with high optical purity.Furthermore, the presence of the tert-butyl group provides steric hindrance, which can influence the reactivity and selectivity of reactions involving the compound. This makes (S)-tert-Butyl 4-(hydroxymethyl)-2,2-dimethyloxazolidine-3-carboxylate a valuable tool for designing efficient synthetic routes with improved yields and selectivity.Overall, the application of (S)-tert-Butyl 4-(hydroxymethyl)-2,2-dimethyloxazolidine-3-carboxylate in chemical synthesis offers chemists a powerful tool for the controlled construction of complex molecules with precise stereochemical control, making it an indispensable asset in the development of new pharmaceuticals and functional materials.
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