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Home  > (R)-N-(tert-Butoxycarbonyl)-tert-leucine

AA29020

124655-17-0 | (R)-N-(tert-Butoxycarbonyl)-tert-leucine

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.

Description
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

 

Computed Properties
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  

 

 

Upstream Synthesis Route
  • 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.
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