(S)-TERT-BUTOXYCARBONYLAMINO-CYCLOPROPYL-ACETIC ACID
Boc-L-cyclopropylglycine
CAS: 155976-13-9
Molecular Formula: C10H17NO4
(S)-TERT-BUTOXYCARBONYLAMINO-CYCLOPROPYL-ACETIC ACID - Names and Identifiers
(S)-TERT-BUTOXYCARBONYLAMINO-CYCLOPROPYL-ACETIC ACID - Physico-chemical Properties
| Molecular Formula | C10H17NO4 |
| Molar Mass | 215.25 |
| Density | 1.206±0.06 g/cm3(Predicted) |
| Melting Point | 79 °C |
| Boling Point | 364.7±25.0 °C(Predicted) |
| Flash Point | 174.373°C |
| Vapor Presure | 0mmHg at 25°C |
| Appearance | Powder |
| Color | White |
| BRN | 6650020 |
| pKa | 3.97±0.10(Predicted) |
| Storage Condition | 2-8°C |
| Refractive Index | 1.508 |
(S)-TERT-BUTOXYCARBONYLAMINO-CYCLOPROPYL-ACETIC ACID - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| WGK Germany | 3 |
| HS Code | 29225090 |
(S)-TERT-BUTOXYCARBONYLAMINO-CYCLOPROPYL-ACETIC ACID - Introduction
Boc-L-cyclopropylglycine is an amino acid derivative and is a white crystalline solid in nature. Its chemical structure contains a L-cyclopropyl glycine group, and there is a protecting group Boc(tert-butyloxycarbonyl) on the amino group.
Boc-L-cyclopropylglycine are widely used in the field of pharmaceutical research and organic synthesis. As one of the amino acids, it can be used in the synthesis of polypeptides and proteins. Its protecting group Boc can protect the active hydrogen atom on the amino group in the chemical reaction to avoid unnecessary reaction. Boc-L-cyclopropylglycine can also be used as building blocks of drug molecules for the synthesis of antibiotics, anti-tumor drugs and other bioactive compounds.
The preparation of Boc-L-cyclopropylglycine is usually carried out by chemical synthesis. A common synthetic method is to react L-cyclopropylglycine with a Boc protecting agent to give Boc-L-cyclopropylglycine. The specific steps of this synthesis method are more complex and require certain organic synthesis techniques and equipment.
Regarding safety information, Boc-L-cyclopropylglycine is usually used in a laboratory environment and is relatively safe when used in accordance with safety operating procedures. However, it may have an irritating effect on the skin, eyes and respiratory tract, so care should be taken to avoid direct contact when using it. In addition, the compound should be stored and handled properly, avoiding contact with acids, oxidants and high temperatures to ensure safe use. In specific use, it is also necessary to refer to the MSDS (safety data sheet) of the compound for detailed safety information.
Boc-L-cyclopropylglycine are widely used in the field of pharmaceutical research and organic synthesis. As one of the amino acids, it can be used in the synthesis of polypeptides and proteins. Its protecting group Boc can protect the active hydrogen atom on the amino group in the chemical reaction to avoid unnecessary reaction. Boc-L-cyclopropylglycine can also be used as building blocks of drug molecules for the synthesis of antibiotics, anti-tumor drugs and other bioactive compounds.
The preparation of Boc-L-cyclopropylglycine is usually carried out by chemical synthesis. A common synthetic method is to react L-cyclopropylglycine with a Boc protecting agent to give Boc-L-cyclopropylglycine. The specific steps of this synthesis method are more complex and require certain organic synthesis techniques and equipment.
Regarding safety information, Boc-L-cyclopropylglycine is usually used in a laboratory environment and is relatively safe when used in accordance with safety operating procedures. However, it may have an irritating effect on the skin, eyes and respiratory tract, so care should be taken to avoid direct contact when using it. In addition, the compound should be stored and handled properly, avoiding contact with acids, oxidants and high temperatures to ensure safe use. In specific use, it is also necessary to refer to the MSDS (safety data sheet) of the compound for detailed safety information.
Last Update：2024-04-09 20:52:54
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View History
(S)-TERT-BUTOXYCARBONYLAMINO-CYCLOPROPYL-ACETIC ACID
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Chrome Yellow G
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哈尔马拉西定碱
二苯甲烷-4,4`-二异氰酸酯
二氯化物
(2,5-DIFLUOROPYRIDIN-3-YL)BORONIC ACID
4-METHYLMORPHOLINE N-OXIDE
4-({6-氨基-2-[(4-氰基苯基)氨基]嘧啶-4-基}氧基)-3,5-二甲基苄腈
Chrome Yellow G
4-(4-BroMophenyl)cyclohexanecarbaldehyde
哈尔马拉西定碱
二苯甲烷-4,4`-二异氰酸酯
二氯化物
(2,5-DIFLUOROPYRIDIN-3-YL)BORONIC ACID
4-METHYLMORPHOLINE N-OXIDE