N-(tert-butoxycarbonyl)-3-cyclohexyl-D-alanine
boc-3-cyclohexyl-D-alanine hydrate
CAS: 127095-92-5
Molecular Formula: C14H25NO4
N-(tert-butoxycarbonyl)-3-cyclohexyl-D-alanine - Names and Identifiers
| Name | boc-3-cyclohexyl-D-alanine hydrate |
| Synonyms | BOC-D-CHA-OH Boc-D-Cha-OH . H2O Boc-D-Cha-OH hydrate BOC-D-3-Cyclohexyl Alanine Boc-(R)-3-Cyclohexylalanine BOC-BETA-CYCLOHEXYL-D-ALA-OH BOC-BETA-CYCLOHEXYL-D-ALANINE (Tert-Butoxy)Carbonyl D-Cha-OH Boc-.beta.-cyclohexyl-D-Ala-OH boc-3-cyclohexyl-D-alanine hydrate BOC-BETA-CYCLOHEXYL-D-ALANINE MONOHYDRATE Boc-beta-cyclohexyl-D-alanine monohydrate Boc-D-Cha-OH OR Boc-3-cyclohexyl-D-alanine (R)-2-(Boc-amino)-3-cyclohexylpropionic Acid N-(tert-butoxycarbonyl)-3-cyclohexyl-D-alanine |
| CAS | 127095-92-5 |
| InChI | InChI=1/C14H25NO4/c1-14(2,3)19-13(18)15-11(12(16)17)9-10-7-5-4-6-8-10/h10-11H,4-9H2,1-3H3,(H,15,18)(H,16,17)/t11-/m1/s1 |
N-(tert-butoxycarbonyl)-3-cyclohexyl-D-alanine - Physico-chemical Properties
| Molecular Formula | C14H25NO4 |
| Molar Mass | 271.35 |
| Density | 1.083g/cm3 |
| Melting Point | 64-67°C |
| Boling Point | 420.4°C at 760 mmHg |
| Flash Point | 208.1°C |
| Vapor Presure | 3.02E-08mmHg at 25°C |
| Storage Condition | Sealed in dry,2-8°C |
| Refractive Index | 1.484 |
N-(tert-butoxycarbonyl)-3-cyclohexyl-D-alanine - Risk and Safety
| WGK Germany | 3 |
| HS Code | 29225090 |
| Hazard Class | IRRITANT |
N-(tert-butoxycarbonyl)-3-cyclohexyl-D-alanine - Introduction
(R)-2-((tert-butoxycarbonyl) amino)-3-cyclohexylpropionic acid is an organic compound often abbreviated as Boc-L-proline. The following is a description of the nature, use, manufacture and safety information of the Boc-L-proline:
Nature:
Boc-L-proline is a white or almost white crystalline solid. It is stable at room temperature and soluble in some organic solvents such as ethanol and dimethylformamide.
Use:
Boc-L-proline is often used in organic synthesis as an amino acid protecting group. It can protect the amino group in the synthesis by removing the protecting group, and then remove the protecting group for subsequent reaction. In addition, Boc-L-proline are also commonly used in drug synthesis, synthetic research, ligand design and other fields.
Method:
The preparation of Boc-L-proline is usually carried out by an organic synthesis method. One common method of preparation is to react L-proline with a tert-butoxycarbonylating agent to give Boc-L-proline.
Safety Information:
Regarding the safety of Boc-L-proline, it should be noted that it may be irritating to the skin, eyes and respiratory system. Avoid inhalation or contact during operation, and take adequate protective measures during operation. Seek medical help immediately if you experience difficulty breathing or discomfort after eye or skin contact. For detailed safety information, refer to the relevant safety data sheet.
Nature:
Boc-L-proline is a white or almost white crystalline solid. It is stable at room temperature and soluble in some organic solvents such as ethanol and dimethylformamide.
Use:
Boc-L-proline is often used in organic synthesis as an amino acid protecting group. It can protect the amino group in the synthesis by removing the protecting group, and then remove the protecting group for subsequent reaction. In addition, Boc-L-proline are also commonly used in drug synthesis, synthetic research, ligand design and other fields.
Method:
The preparation of Boc-L-proline is usually carried out by an organic synthesis method. One common method of preparation is to react L-proline with a tert-butoxycarbonylating agent to give Boc-L-proline.
Safety Information:
Regarding the safety of Boc-L-proline, it should be noted that it may be irritating to the skin, eyes and respiratory system. Avoid inhalation or contact during operation, and take adequate protective measures during operation. Seek medical help immediately if you experience difficulty breathing or discomfort after eye or skin contact. For detailed safety information, refer to the relevant safety data sheet.
Last Update：2024-04-09 19:05:46
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