AE16091
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
100mg | 99% | in stock | $89.00 | $62.00 | - + | |
250mg | 99% | in stock | $152.00 | $107.00 | - + | |
1g | 99% | in stock | $287.00 | $201.00 | - + | |
5g | 99% | in stock | $1,062.00 | $743.00 | - + | |
10g | 99% | in stock | $1,989.00 | $1,393.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AE16091 |
Chemical Name: | (S)-Boc-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid |
CAS Number: | 112898-19-8 |
Molecular Formula: | C11H19NO4S |
Molecular Weight: | 261.3379 |
MDL Number: | MFCD00070265 |
SMILES: | OC(=O)[C@@H]1N(CSC1(C)C)C(=O)OC(C)(C)C |
(S)-3-(tert-Butoxycarbonyl)-5,5-dimethylthiazolidine-4-carboxylic acid, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound plays a crucial role in asymmetric synthesis, particularly in the preparation of chiral molecules.One important application of (S)-3-(tert-Butoxycarbonyl)-5,5-dimethylthiazolidine-4-carboxylic acid is as a chiral auxiliary in various reactions. By attaching this compound to a substrate, chemists are able to control the stereochemistry of the resulting products. This is essential in the synthesis of pharmaceuticals, agrochemicals, and other complex organic molecules where chirality is a determining factor in biological activity.Additionally, (S)-3-(tert-Butoxycarbonyl)-5,5-dimethylthiazolidine-4-carboxylic acid can also act as a protecting group for amines in organic synthesis. This allows chemists to selectively manipulate certain functional groups in a molecule while keeping the amine group protected until needed. This versatility makes (S)-3-(tert-Butoxycarbonyl)-5,5-dimethylthiazolidine-4-carboxylic acid a valuable tool in the synthetic chemist's toolbox.Overall, (S)-3-(tert-Butoxycarbonyl)-5,5-dimethylthiazolidine-4-carboxylic acid is an essential compound in the field of chemical synthesis, enabling the creation of complex and chiral molecules with precision and control.