(2S)-[(tert-butoxycarbonyl)amino](cyclopentyl)ethanoic acid
Boc-L-Cyclopentylglycine
CAS: 109183-72-4
Molecular Formula: C12H21NO4
(2S)-[(tert-butoxycarbonyl)amino](cyclopentyl)ethanoic acid - Names and Identifiers
(2S)-[(tert-butoxycarbonyl)amino](cyclopentyl)ethanoic acid - Physico-chemical Properties
| Molecular Formula | C12H21NO4 |
| Molar Mass | 243.3 |
| Density | 1.137±0.06 g/cm3(Predicted) |
| Boling Point | 393.5±25.0 °C(Predicted) |
| Flash Point | 191.8°C |
| Vapor Presure | 2.74E-07mmHg at 25°C |
| Appearance | Powder |
| Color | White |
| pKa | 4.06±0.10(Predicted) |
| Storage Condition | Sealed in dry,Room Temperature |
| Refractive Index | 1.494 |
| Physical and Chemical Properties | Storage Conditions:-15 ℃ |
(2S)-[(tert-butoxycarbonyl)amino](cyclopentyl)ethanoic acid - Risk and Safety
| HS Code | 29225090 |
| Hazard Class | IRRITANT |
(2S)-[(tert-butoxycarbonyl)amino](cyclopentyl)ethanoic acid - Introduction
Boc-L-Cyclopentylglycine is an organic compound with the following properties:
Appearance: Boc-L-Cyclopentylglycine is usually a white or off-white solid.
Solubility: Boc-L-Cyclopentylglycine is soluble in common organic solvents such as chloroform, dimethylformamide and methanol.
Purpose: Boc-L-cyclopentylglycine is commonly used in the synthesis of peptides and proteins. It can be used as a protecting group to protect the carboxyl group of the amino acid to control the selectivity and stereochemistry of the reaction. In addition, Boc-L-cyclopentylglycine can also be used for the synthesis of other compounds in drug development and organic synthesis.
Preparation Method: The synthesis of Boc-L-cyclopentylglycine usually uses L-cyclopentylglycine as a raw material. First, L-cyclopentylglycine is reacted with t-butoxycarbenoic acid (BOC-OH) to give a BOC-protected ester of Boc-L-cyclopentylglycine. Then, the protecting group is removed by a hydrogenation reaction, thereby obtaining Boc-L-cyclopentylglycine.
Safety Information: Boc-L-Cyclopentylglycine is less dangerous when used correctly. However, it is a chemical and attention should be paid to safe handling. During the treatment, direct contact with skin and eyes should be avoided, and a well-ventilated working environment should be maintained. In addition, it should be stored in a dry, cool place, away from fire and oxidizing agents. Detailed safety operation instructions should refer to the relevant safety data sheets on a case-by-case basis.
Appearance: Boc-L-Cyclopentylglycine is usually a white or off-white solid.
Solubility: Boc-L-Cyclopentylglycine is soluble in common organic solvents such as chloroform, dimethylformamide and methanol.
Purpose: Boc-L-cyclopentylglycine is commonly used in the synthesis of peptides and proteins. It can be used as a protecting group to protect the carboxyl group of the amino acid to control the selectivity and stereochemistry of the reaction. In addition, Boc-L-cyclopentylglycine can also be used for the synthesis of other compounds in drug development and organic synthesis.
Preparation Method: The synthesis of Boc-L-cyclopentylglycine usually uses L-cyclopentylglycine as a raw material. First, L-cyclopentylglycine is reacted with t-butoxycarbenoic acid (BOC-OH) to give a BOC-protected ester of Boc-L-cyclopentylglycine. Then, the protecting group is removed by a hydrogenation reaction, thereby obtaining Boc-L-cyclopentylglycine.
Safety Information: Boc-L-Cyclopentylglycine is less dangerous when used correctly. However, it is a chemical and attention should be paid to safe handling. During the treatment, direct contact with skin and eyes should be avoided, and a well-ventilated working environment should be maintained. In addition, it should be stored in a dry, cool place, away from fire and oxidizing agents. Detailed safety operation instructions should refer to the relevant safety data sheets on a case-by-case basis.
Last Update：2024-04-09 21:01:54
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Product Name: Boc-Cyclopentyl-Gly-OH Dcha Visit Supplier Webpage Request for quotation
CAS: 109183-72-4
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QQ: 3008007409
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CAS: 109183-72-4
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View History
(2S)-[(tert-butoxycarbonyl)amino](cyclopentyl)ethanoic acid
3-acetyl-8-chloro-2-phenylquinolin-4(1H)-one
3-acetyl-8-chloro-2-phenylquinolin-4(1H)-one