Carbamic acid, (2-amino-1-phenylethyl)-, 1,1-dimethylethyl ester, (R)-
(R)-2-(Boc-amino)-2-phenylethylamine
CAS: 137102-65-9
Molecular Formula: C13H20N2O2
Carbamic acid, (2-amino-1-phenylethyl)-, 1,1-dimethylethyl ester, (R)- - Names and Identifiers
Carbamic acid, (2-amino-1-phenylethyl)-, 1,1-dimethylethyl ester, (R)- - Physico-chemical Properties
| Molecular Formula | C13H20N2O2 |
| Molar Mass | 236.31 |
| Density | 1.066±0.06 g/cm3(Predicted) |
| Boling Point | 372.2±35.0 °C(Predicted) |
| pKa | 11?+-.0.46(Predicted) |
| Storage Condition | Room Temprature |
Carbamic acid, (2-amino-1-phenylethyl)-, 1,1-dimethylethyl ester, (R)- - Introduction
(S)-tert-butyl N-(2-amino-1-phenylethyl) carbamate is often referred to simply as Boc-NH-L-Phg-OBut. The following is a description of some properties, uses, preparation and safety information about the substance:
Properties: Boc-NH-L-Phg-OBut is a colorless to pale yellow crystalline solid with low solubility. It is stable under normal conditions, but is more sensitive to acids and alkalis. Its molecular formula is C18H26N2O3 and its relative molecular mass is 318.41g/mol.
Uses: The main use of Boc-NH-L-Phg-OBut is as a protecting group (reagent) in organic synthesis. It can be used in the synthesis of natural products, drug molecules and complex organic compounds. Protecting groups can prevent the reaction of specific functional groups in the target molecule and can be deprotected when necessary.
Preparation method: The preparation of Boc-NH-L-Phg-OBut is usually achieved by chemical synthesis. One common method involves the esterification of Boc-NH-L-Phg with tert-butanol. The reaction is usually carried out in the presence of a suitable solvent and an acid catalyst.
Safety Information: Boc-NH-L-Phg-OBut should be operated under appropriate laboratory conditions. Its toxicity to humans is not known, but inhalation, skin contact and ingestion should be avoided. During use, protective gloves and glasses should be worn and good ventilation should be ensured. In case of accident or discomfort, seek medical attention immediately. In addition, the Boc-NH-L-Phg-OBut should be stored in a dry, cool and sealed container, away from fire and oxidizing agents.
Properties: Boc-NH-L-Phg-OBut is a colorless to pale yellow crystalline solid with low solubility. It is stable under normal conditions, but is more sensitive to acids and alkalis. Its molecular formula is C18H26N2O3 and its relative molecular mass is 318.41g/mol.
Uses: The main use of Boc-NH-L-Phg-OBut is as a protecting group (reagent) in organic synthesis. It can be used in the synthesis of natural products, drug molecules and complex organic compounds. Protecting groups can prevent the reaction of specific functional groups in the target molecule and can be deprotected when necessary.
Preparation method: The preparation of Boc-NH-L-Phg-OBut is usually achieved by chemical synthesis. One common method involves the esterification of Boc-NH-L-Phg with tert-butanol. The reaction is usually carried out in the presence of a suitable solvent and an acid catalyst.
Safety Information: Boc-NH-L-Phg-OBut should be operated under appropriate laboratory conditions. Its toxicity to humans is not known, but inhalation, skin contact and ingestion should be avoided. During use, protective gloves and glasses should be worn and good ventilation should be ensured. In case of accident or discomfort, seek medical attention immediately. In addition, the Boc-NH-L-Phg-OBut should be stored in a dry, cool and sealed container, away from fire and oxidizing agents.
Last Update：2024-04-09 20:52:54
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Product Name: [(1R)-2-AMINO-1-PHENYLETHYL]-CARBAMIC ACID 1,1-DIMETHYLETHYL ESTER Visit Supplier Webpage Request for quotation
CAS: 137102-65-9
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Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
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CAS: 137102-65-9
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
View History
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