AA29020
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 97% | in stock | $14.00 | $10.00 | - + | |
1g | 97% | in stock | $25.00 | $17.00 | - + | |
5g | 97% | in stock | $32.00 | $22.00 | - + | |
10g | 97% | in stock | $39.00 | $27.00 | - + | |
25g | 97% | in stock | $65.00 | $45.00 | - + | |
100g | 97% | in stock | $252.00 | $176.00 | - + | |
500g | 97% | in stock | $1,007.00 | $705.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA29020 |
Chemical Name: | (R)-N-(tert-Butoxycarbonyl)-tert-leucine |
CAS Number: | 124655-17-0 |
Molecular Formula: | C11H21NO4 |
Molecular Weight: | 231.2887 |
MDL Number: | MFCD00065575 |
SMILES: | O=C(OC(C)(C)C)N[C@H](C(C)(C)C)C(=O)O |
Complexity: | 273 |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 1 |
Heavy Atom Count: | 16 |
Hydrogen Bond Acceptor Count: | 4 |
Hydrogen Bond Donor Count: | 2 |
Rotatable Bond Count: | 5 |
XLogP3: | 2.3 |
N-(tert-Butoxycarbonyl)-D-tert-leucine, also known as Boc-D-tert-leucine, is a valuable compound widely utilized in chemical synthesis. This compound serves as a versatile building block in peptide synthesis, specifically for the protection of amino groups in peptide chains. By selectively shielding the N-terminal amino group with the Boc (tert-butoxycarbonyl) group, Boc-D-tert-leucine enables controlled and sequential peptide bond formation during the synthesis process.In addition to its role in peptide chemistry, Boc-D-tert-leucine is also employed in the production of pharmaceutical intermediates and fine chemicals. Its compatibility with a variety of reaction conditions and its stability make it a preferred reagent in organic synthesis. Furthermore, the tert-butyl ester group can be easily removed under mild acidic conditions, allowing for the efficient deprotection of the amino group and subsequent modifications.Overall, N-(tert-Butoxycarbonyl)-D-tert-leucine plays a crucial function in the synthesis of complex peptides and organic molecules, offering chemists a reliable tool for the precise manipulation of amino acids and facilitating the creation of diverse chemical structures.