Boc-N-Me-D-Ala-OH NEW
Price | Get Latest Price | ||
Package | 1kg | 10kg | 100kg |
Min. Order: | 1kg |
Supply Ability: | 1T+ |
Update Time: | 2024-12-26 |
Product Details
Product Name: Boc-N-Me-D-Ala-OH | CAS No.: 19914-38-6 |
Min. Order: 1kg | Purity: 98% |
Supply Ability: 1T+ | Release date: 2024/12/26 |
Product Name: | Boc-N-Me-D-Ala-OH |
CAS: | 19914-38-6 |
MF: | C9H17NO4 |
MW: | 203.24 |
Synonyms: | N-(tert-Butoxycarbonyl)-N-methyl-D-alanine;BOC-N-ME-D-ALA-OH;BOC-N-ME-R-ALA-OH;BOC-N-METHYL-D-ALANINE;BOC-N-ALPHA-METHYL-D-ALANINE;BOC-D-MEALA-OH;BOC-D-N-ME-ALA-OH;N-ALPHA-T-BOC-N-ALPHA-METHYL-D-ALANINE |
Product Categories: | Amino Acid Derivatives; Amino Acid Esters |
Application: | Peptide Synthesis: Boc-N-Me-D-Ala-OH serves as a protected form of N-methyl-D-alanine, a modified form of alanine. It is utilized in the assembly of peptides, particularly in solid-phase peptide synthesis (SPPS). The Boc group protects the amino terminus of alanine, while the N-methyl group introduces structural and chemical modifications to the peptide. Solid-phase Peptide Synthesis (SPPS): In SPPS, Boc-N-Me-D-Ala-OH can be immobilized onto a solid support and used for sequential elongation of peptide chains. After each coupling reaction, the Boc group is selectively removed under mild conditions, exposing the amino group of alanine for the next coupling reaction. Peptidomimetics: This compound can be used in the synthesis of peptidomimetics, which are molecules designed to mimic the structure and function of peptides. Peptidomimetics often possess improved stability, bioavailability, or other advantageous properties compared to peptides, making them valuable in drug discovery and development. |
Manufacturer: | Sichuan HongRi Pharma-Tech Co., Ltd. |
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- Since: 2021-03-30
- Address: A38-2, No. 66, Nanhu road, Deyang City, Sichuan Province (Jiuwei Blue Valley)