N-ALPHA-TERT-BUTYLOXYCARBONYL-N-BETA-(9-FLUORENYLMETHYLOXYCARBONYL)-D-2,3-DIAMINOPROPIONIC ACID
Boc-D-Dap(Fmoc)-OH
CAS: 131570-56-4
Molecular Formula: C23H26N2O6
N-ALPHA-TERT-BUTYLOXYCARBONYL-N-BETA-(9-FLUORENYLMETHYLOXYCARBONYL)-D-2,3-DIAMINOPROPIONIC ACID - Names and Identifiers
N-ALPHA-TERT-BUTYLOXYCARBONYL-N-BETA-(9-FLUORENYLMETHYLOXYCARBONYL)-D-2,3-DIAMINOPROPIONIC ACID - Physico-chemical Properties
| Molecular Formula | C23H26N2O6 |
| Molar Mass | 426.46 |
| Density | 1.263±0.06 g/cm3(Predicted) |
| Boling Point | 652.5±55.0 °C(Predicted) |
| Water Solubility | Slightly soluble in water. |
| Appearance | White powder |
| pKa | 3?+-.0.10(Predicted) |
| Storage Condition | Sealed in dry,2-8°C |
| MDL | MFCD00236844 |
N-ALPHA-TERT-BUTYLOXYCARBONYL-N-BETA-(9-FLUORENYLMETHYLOXYCARBONYL)-D-2,3-DIAMINOPROPIONIC ACID - Risk and Safety
| HS Code | 29225090 |
N-ALPHA-TERT-BUTYLOXYCARBONYL-N-BETA-(9-FLUORENYLMETHYLOXYCARBONYL)-D-2,3-DIAMINOPROPIONIC ACID - Introduction
N-tert-butoxycarbonyl-N'-fluorenylmethoxycarbonyl-D-2, 3-diaminopropionic acid is an organic compound whose molecular formula is C21H28N4O5. The following is a description of the properties, uses, preparation and safety information of the compound:
Nature:
-Appearance: Colorless solid
-melting point: about 155-160 ℃
-Solubility: Soluble in common organic solvents, such as methanol, dimethyl sulfoxide, etc.
-Stability: relatively stable at room temperature, but unstable under strong acid and alkali conditions
-Polarity: Due to the functional groups such as fluorenyl and carbonyl, it has a certain polarity
Use:
- N-tert-butoxycarbonyl-N'-fluorenylmethoxycarbonyl-D-2, 3-diaminopropionic acid is a deprotecting reagent, which is often used to remove amino protecting groups in organic chemical synthesis in order to obtain Target molecules.
Preparation Method:
-The compound can usually be obtained by chemical synthesis methods. The specific methods are as follows: First, a suitable starting material is reacted with a suitable reagent under suitable reaction conditions to generate an intermediate; then, the intermediate is further processed, Such as the introduction or elimination of protecting groups, the esterification of hydroxyl groups, etc.; finally, after a series of reaction and purification procedures, finally, N-tert-butoxycarbonyl-N'-fluorenylmethoxycarbonyl-D-2, 3-diaminopropionic acid is obtained.
Security Information:
-The compound is generally safe to use under proper handling and storage conditions.
-Due to the nature of its deprotection reagent, it is necessary to pay attention to the selection of suitable conditions when used in organic synthesis.
-When using or handling the compound, follow appropriate laboratory safety practices, including wearing personal protective equipment (e. g., lab gloves, goggles).
-This compound may be irritating to the skin, eyes and respiratory system. Avoid contact with skin or inhalation of its volatiles.
-During use and storage, keep away from fire and high temperature to prevent hazards such as combustion and explosion.
Nature:
-Appearance: Colorless solid
-melting point: about 155-160 ℃
-Solubility: Soluble in common organic solvents, such as methanol, dimethyl sulfoxide, etc.
-Stability: relatively stable at room temperature, but unstable under strong acid and alkali conditions
-Polarity: Due to the functional groups such as fluorenyl and carbonyl, it has a certain polarity
Use:
- N-tert-butoxycarbonyl-N'-fluorenylmethoxycarbonyl-D-2, 3-diaminopropionic acid is a deprotecting reagent, which is often used to remove amino protecting groups in organic chemical synthesis in order to obtain Target molecules.
Preparation Method:
-The compound can usually be obtained by chemical synthesis methods. The specific methods are as follows: First, a suitable starting material is reacted with a suitable reagent under suitable reaction conditions to generate an intermediate; then, the intermediate is further processed, Such as the introduction or elimination of protecting groups, the esterification of hydroxyl groups, etc.; finally, after a series of reaction and purification procedures, finally, N-tert-butoxycarbonyl-N'-fluorenylmethoxycarbonyl-D-2, 3-diaminopropionic acid is obtained.
Security Information:
-The compound is generally safe to use under proper handling and storage conditions.
-Due to the nature of its deprotection reagent, it is necessary to pay attention to the selection of suitable conditions when used in organic synthesis.
-When using or handling the compound, follow appropriate laboratory safety practices, including wearing personal protective equipment (e. g., lab gloves, goggles).
-This compound may be irritating to the skin, eyes and respiratory system. Avoid contact with skin or inhalation of its volatiles.
-During use and storage, keep away from fire and high temperature to prevent hazards such as combustion and explosion.
Last Update：2024-04-10 22:29:15
Supplier List
Product Name: (R)-2-(Boc-amino)-3-(Fmoc-amino)propionic acid Visit Supplier Webpage Request for quotation
CAS: 131570-56-4
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
CAS: 131570-56-4
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
Product Name: (R)-2-(Boc-amino)-3-(Fmoc-amino)propionic acid Visit Supplier Webpage Request for quotation
CAS: 131570-56-4
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
CAS: 131570-56-4
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
View History