166410-05-5
BOC-4-OXO-L-PROLINE TERT-BUTYL ESTER
CAS: 166410-05-5
Molecular Formula: C14H23NO5
166410-05-5 - Names and Identifiers
| Name | BOC-4-OXO-L-PROLINE TERT-BUTYL ESTER |
| Synonyms | K204 Boc-4-OXO-Pro-OtBu BOC-4-OXO-L-PROLINE TERT-BUTYL ESTER N-BOC-4-OXO-L-PROLINE TERT-BUTYL ESTER 1-(tert-butoxycarbonyl)-4-oxo-L-proline N-T-BOC-4-OXO-L-PROLINE TERT-BUTYL ESTER ditert-butyl (2S)-4-oxopyrrolidine-1,2-dicarboxylate di-tert-butyl (2S)-4-oxopyrrolidine-1,2-dicarboxylate (2S) tert-butyl N-(tert-butoxycabonyl)-4-oxoprolinate 1,2-di-tert-butyl (2S)-4-oxopyrrolidine-1,2- dicarboxylate |
| CAS | 166410-05-5 |
| InChI | InChI=1/C10H15NO5/c1-10(2,3)16-9(15)11-5-6(12)4-7(11)8(13)14/h7H,4-5H2,1-3H3,(H,13,14)/t7-/m0/s1 |
166410-05-5 - Physico-chemical Properties
| Molecular Formula | C14H23NO5 |
| Molar Mass | 285.34 |
| Density | 1.138±0.06 g/cm3(Predicted) |
| Melting Point | 64-67°C |
| Boling Point | 366.7±42.0 °C(Predicted) |
| Flash Point | 190.123°C |
| Vapor Presure | 0mmHg at 25°C |
| pKa | -3.86±0.40(Predicted) |
| Storage Condition | Sealed in dry,Store in freezer, under -20°C |
| Refractive Index | 1.516 |
166410-05-5 - Introduction
BOC-4-OXO-L-PROLINE TERT-BUTYL ESTER is an organic compound with the chemical formula C13H21NO6. It is a white solid, stable at room temperature. The following describes its nature, use, preparation and safety information:
Nature:
BOC-4-OXO-L-PROLINE TERT-BUTYL ESTER has low solubility and is soluble in organic solvents such as dimethylformamide (DMF) and dichloromethane. It is a stable compound that does not easily decompose at room temperature. Its molecular structure contains oxygen (-COOR) and Boc protecting groups, which make it have certain chemical activity in organic synthesis.
Use:
BOC-4-OXO-L-PROLINE TERT-BUTYL ESTER is often used as an intermediate in organic synthesis. Because its structure contains amino acid groups, it is often used in the synthesis of peptide compounds. By controlling the reaction conditions, the Boc protecting group can be removed to obtain a free amino acid, which can be used to synthesize natural proteins, drugs and other biologically active molecules.
Method:
There are many methods for preparing BOC-4-OXO-L-PROLINE TERT-BUTYL ESTER. One common method is to acidify proline with tert-butyl alcohol to generate proline tert-butyl ESTER, and then esterify it with acetic anhydride to generate BOC-4-OXO-L-PROLINE TERT-BUTYL ESTER.
Safety Information:
BOC-4-OXO-L-PROLINE TERT-BUTYL ESTER is a relatively safe compound under normal use conditions. However, it is subject to some regular laboratory safety measures. Wear suitable personal protective equipment such as laboratory gloves and goggles when handling the compound. At the same time, it should be operated under well-ventilated laboratory conditions to avoid its potential impact on the human body and the environment.
Nature:
BOC-4-OXO-L-PROLINE TERT-BUTYL ESTER has low solubility and is soluble in organic solvents such as dimethylformamide (DMF) and dichloromethane. It is a stable compound that does not easily decompose at room temperature. Its molecular structure contains oxygen (-COOR) and Boc protecting groups, which make it have certain chemical activity in organic synthesis.
Use:
BOC-4-OXO-L-PROLINE TERT-BUTYL ESTER is often used as an intermediate in organic synthesis. Because its structure contains amino acid groups, it is often used in the synthesis of peptide compounds. By controlling the reaction conditions, the Boc protecting group can be removed to obtain a free amino acid, which can be used to synthesize natural proteins, drugs and other biologically active molecules.
Method:
There are many methods for preparing BOC-4-OXO-L-PROLINE TERT-BUTYL ESTER. One common method is to acidify proline with tert-butyl alcohol to generate proline tert-butyl ESTER, and then esterify it with acetic anhydride to generate BOC-4-OXO-L-PROLINE TERT-BUTYL ESTER.
Safety Information:
BOC-4-OXO-L-PROLINE TERT-BUTYL ESTER is a relatively safe compound under normal use conditions. However, it is subject to some regular laboratory safety measures. Wear suitable personal protective equipment such as laboratory gloves and goggles when handling the compound. At the same time, it should be operated under well-ventilated laboratory conditions to avoid its potential impact on the human body and the environment.
Last Update：2024-04-09 21:11:58
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Featured ProductsSpot supply
Product Name: BOC-4-OXO-L-PROLINE TERT-BUTYL ESTER Visit Supplier Webpage Request for quotationCAS: 166410-05-5
Tel: +86-18821248368
Email: Int06@meryer.com
Mobile: +86-18821248368
QQ: 495145328
WhatsApp: +86-18821248368
Spot supply
Product Name: (S)-Di-tert-butyl4-oxopyrrolidine-1,2-dicarboxylate Request for quotationCAS: 166410-05-5
Tel: 400-968-2212
Email: 3623107365@qq.com
Mobile: 18916960931
QQ: 3623107365
Wechat: 18916960931
Spot supply
Product Name: N-Boc-4-oxo-L-proline tert-butyl ester, 97% Visit Supplier Webpage Request for quotationCAS: 166410-05-5
Tel: +86-400-900-4166
Email: product@acmec-e.com
Mobile: +86-18621343501
QQ: 2881950922
Wechat: 18621343501
WhatsApp: +86-18621343501
View History
166410-05-5
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136483-17-5
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Monochlororesorcinol
136483-17-5
1516-08-1
crotylidene acetic acid
Γ-苯丁酸
50505-61-8
carbane-13
氨基甲酸铵
对二乙酰苯