3-(Benzylamino)-D-alanine
3-(Benzylamino)-D-alanine
CAS: 119906-14-5
Molecular Formula: C10H14N2O2
3-(Benzylamino)-D-alanine - Names and Identifiers
| Name | 3-(Benzylamino)-D-alanine |
| Synonyms | 3-(Benzylamino)-D-alanine D-β-(N-benzylamino) alanine D-SS-(N-BENZYLAMINO)ALANINE D-beta-(N-benzylamino)alanine D-BETA-(N-BENZYLAMINO)ALANINE |
| CAS | 119906-14-5 |
| InChI | InChI=1S/C10H14N2O2/c11-9(10(13)14)7-12-6-8-4-2-1-3-5-8/h1-5,9,12H,6-7,11H2,(H,13,14)/t9-/m1/s1 |
3-(Benzylamino)-D-alanine - Physico-chemical Properties
| Molecular Formula | C10H14N2O2 |
| Molar Mass | 194.23036 |
3-(Benzylamino)-D-alanine - Introduction
D-B-(N-benzylamino) alanine, also known as Boc-D-Beta-(N-benzyloxycarbonyl amino)alanine, is an unnatural amino acid. The following is an introduction to its nature, use, formulation and safety information:
Nature:
D-B-(N-benzylamino) alanine is a white crystalline solid, soluble in some organic solvents such as methanol, chloroform and dimethyl sulfoxide. It is a chiral molecule with a D configuration.
Use:
D-B-(N-benzylamino) alanine is commonly used in peptide synthesis in chemical synthesis as a building block for peptide chains. It can be used to synthesize peptide drugs with biological activity, such as peptide hormones, peptide liberation factors or antimicrobial peptides.
Preparation Method:
The preparation of D-B-(N-benzylamino) alanine is usually achieved by chemical synthesis methods. This synthesis usually includes the following steps: first, anisole is added to β-aminopropionic acid by an appropriate chemical reaction to form a N-benzyl protecting group; then, a carbon monoxide group (Boc) is added to the amino group by an appropriate reaction to form a Boc protecting group; finally, the target product D-B-(N-benzylamino) alanine is obtained by a series of reaction and purification steps.
Safety Information:
D-Β-(N-benzylamino) alanine has no obvious toxicity to human body under normal conditions. However, during handling and use, laboratory safety procedures should be followed to avoid direct contact with skin and inhalation. At the same time, the storage and use environment should be kept well ventilated, away from fire and oxidant. It is best to use under professional laboratory conditions and follow relevant safety guidelines and regulations.
Nature:
D-B-(N-benzylamino) alanine is a white crystalline solid, soluble in some organic solvents such as methanol, chloroform and dimethyl sulfoxide. It is a chiral molecule with a D configuration.
Use:
D-B-(N-benzylamino) alanine is commonly used in peptide synthesis in chemical synthesis as a building block for peptide chains. It can be used to synthesize peptide drugs with biological activity, such as peptide hormones, peptide liberation factors or antimicrobial peptides.
Preparation Method:
The preparation of D-B-(N-benzylamino) alanine is usually achieved by chemical synthesis methods. This synthesis usually includes the following steps: first, anisole is added to β-aminopropionic acid by an appropriate chemical reaction to form a N-benzyl protecting group; then, a carbon monoxide group (Boc) is added to the amino group by an appropriate reaction to form a Boc protecting group; finally, the target product D-B-(N-benzylamino) alanine is obtained by a series of reaction and purification steps.
Safety Information:
D-Β-(N-benzylamino) alanine has no obvious toxicity to human body under normal conditions. However, during handling and use, laboratory safety procedures should be followed to avoid direct contact with skin and inhalation. At the same time, the storage and use environment should be kept well ventilated, away from fire and oxidant. It is best to use under professional laboratory conditions and follow relevant safety guidelines and regulations.
Last Update：2024-04-09 21:32:37
