Boc-(S)-3-Cyclopropylalanine DCHA
Boc-.beta.-cyclopropyl-Ala-OH . DCHA
CAS: 89483-07-8
Molecular Formula: C23H42N2O4
Boc-(S)-3-Cyclopropylalanine DCHA - Names and Identifiers
| Name | Boc-.beta.-cyclopropyl-Ala-OH . DCHA |
| Synonyms | Boc-L-Cyclopropylalanine.DCHA Boc-L-Cyclopropylalanine-Dcha N-TBOC-B-CYCLOPROPYL-L-ALANINE BOC-BETA-CYCLOPROPYL-ALA-OH DCHA Boc-(S)-3-Cyclopropylalanine DCHA BOC-BETA-CYCLOPROPYL-ALANINE DCHA BOC-BETA-CYCLOPROPYL-L-ALA-OH DCHA BOC-BETA-CYCLOPROPYL-L-ALANINE DCHA Boc-.beta.-cyclopropyl-Ala-OH . DCHA Boc-L-Cyclopropylalanine dicyclohexylamine salt N-(tert-butoxycarbonyl)-3-cyclopropyl-L-alanine BOC-ALA(BETA-CYCLOPROPYL)-OH DICYCLOHEXYLAMMONIUM SALT |
| CAS | 89483-07-8 |
| InChI | InChI=1/C11H19NO4/c1-11(2,3)16-10(15)12-8(9(13)14)6-7-4-5-7/h7-8H,4-6H2,1-3H3,(H,12,15)(H,13,14)/t8-/m0/s1 |
Boc-(S)-3-Cyclopropylalanine DCHA - Physico-chemical Properties
| Molecular Formula | C23H42N2O4 |
| Molar Mass | 410.59 |
| Density | 1.162g/cm3 |
| Boling Point | 377.2°C at 760 mmHg |
| Flash Point | 181.9°C |
| Vapor Presure | 9.93E-07mmHg at 25°C |
| Storage Condition | under inert gas (nitrogen or Argon) at 2-8°C |
| Refractive Index | 1.498 |
| MDL | MFCD03093869 |
Boc-(S)-3-Cyclopropylalanine DCHA - Risk and Safety
| Hazard Class | IRRITANT |
Boc-(S)-3-Cyclopropylalanine DCHA - Introduction
Boc-.beta.-cyclopropyl-Ala-OH . DCHA(Boc-.beta.-cyclopropyl-Ala-OH . DCHA) is an organic compound. The following is a description of its nature, use, formulation and safety information:
Nature:
-Appearance: a solid powder
-Molecular formula: C18H29NO4
-Molecular weight: 323.43g/mol
-Melting point: about 50-55 degrees Celsius
Use:
- Boc-.beta.-cyclopropyl-Ala-OH . DCHA is a commonly used amino acid derivative, commonly used in pharmaceutical chemical synthesis.
-It can be modified as a drug active group for the synthesis of peptide drugs or other biologically active molecules.
-Because it has the characteristics of cyclopropyl structure, it may have unique biological activity and selectivity in drug design.
Preparation Method:
- Boc-.beta.-cyclopropyl-Ala-OH . DCHA can be prepared by chemical synthesis.
-A common method is to first synthesize N-tert-butoxycarbonyl-L-cyclopropylalanine, and then react with dicyclohexylamine to form dicyclohexylamine salt.
Safety Information:
- Boc-.beta.-cyclopropyl-Ala-OH . DCHA is generally considered to be relatively safe under normal conditions.
-When handling this compound, follow laboratory safety practices, including wearing appropriate protective equipment (such as gloves and glasses).
-If ingested or exposed to this compound, seek medical help immediately and provide detailed information to your doctor.
-When storing this compound, keep it in a dry, cool place and away from combustibles and oxidants.
Nature:
-Appearance: a solid powder
-Molecular formula: C18H29NO4
-Molecular weight: 323.43g/mol
-Melting point: about 50-55 degrees Celsius
Use:
- Boc-.beta.-cyclopropyl-Ala-OH . DCHA is a commonly used amino acid derivative, commonly used in pharmaceutical chemical synthesis.
-It can be modified as a drug active group for the synthesis of peptide drugs or other biologically active molecules.
-Because it has the characteristics of cyclopropyl structure, it may have unique biological activity and selectivity in drug design.
Preparation Method:
- Boc-.beta.-cyclopropyl-Ala-OH . DCHA can be prepared by chemical synthesis.
-A common method is to first synthesize N-tert-butoxycarbonyl-L-cyclopropylalanine, and then react with dicyclohexylamine to form dicyclohexylamine salt.
Safety Information:
- Boc-.beta.-cyclopropyl-Ala-OH . DCHA is generally considered to be relatively safe under normal conditions.
-When handling this compound, follow laboratory safety practices, including wearing appropriate protective equipment (such as gloves and glasses).
-If ingested or exposed to this compound, seek medical help immediately and provide detailed information to your doctor.
-When storing this compound, keep it in a dry, cool place and away from combustibles and oxidants.
Last Update：2024-04-09 15:18:00
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