N-boc-dl-2-氨基丁酸
(2R)-2-[(tert-butoxycarbonyl)amino]butanoate
CAS: 77284-64-1
Molecular Formula: C9H17NO4
N-boc-dl-2-氨基丁酸 - Names and Identifiers
| Name | (2R)-2-[(tert-butoxycarbonyl)amino]butanoate |
| Synonyms | Boc-DL-2-Abu Boc-2-aminobutyric acid Boc-2-aMinobutyric acid DL-Boc-Aminobutyric acid BOC-DL-2-AMINOBUTYRIC ACID 2-(tert-butoxycarbonyl)butanoic acid 2-Aminobutanoic acid, N-BOC protected 2-[(tert-Butoxycarbonyl)amino]butanoic acid (2R)-2-[(tert-butoxycarbonyl)amino]butanoate Butanoic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]- |
| CAS | 77284-64-1 |
| InChI | InChI=1/C9H17NO4/c1-5-6(7(11)12)10-8(13)14-9(2,3)4/h6H,5H2,1-4H3,(H,10,13)(H,11,12)/p-1/t6-/m1/s1 |
N-boc-dl-2-氨基丁酸 - Physico-chemical Properties
| Molecular Formula | C9H17NO4 |
| Molar Mass | 203.24 |
| Density | 1.101±0.06 g/cm3(Predicted) |
| Melting Point | 60-62 °C |
| Boling Point | 334.5±25.0 °C(Predicted) |
| Flash Point | 156.1°C |
| Vapor Presure | 2.42E-05mmHg at 25°C |
| pKa | 4.00±0.10(Predicted) |
| Storage Condition | Sealed in dry,Room Temperature |
N-boc-dl-2-氨基丁酸 - Risk and Safety
| Hazard Class | IRRITANT |
N-boc-dl-2-氨基丁酸 - Introduction
(2R)-2-[(tert-butoxycarbonyl)amino]butanoate, chemical formula C11H21NO4, is an organic compound. It is a white solid with a low melting and boiling point.
(2R)-2-[(tert-butoxycarbonyl)amino]butanoate is widely used in organic synthesis. It is often used as a reagent for protecting amine groups, I .e., an amino group as a Boc group. This protection prevents the amine group from participating in the reaction and also improves the stability of the compound. In synthetic chemistry, various drugs, additives and functional molecules can be synthesized using (2R)-2-[(tert-butoxycarbonyl)amino]butanoate.
The method for preparing (2R)-2-[(tert-butoxycarbonyl)amino]butanoate is usually obtained by reacting 2-aminobutyric acid with tert-butyl carbonate for esterification. The specific synthetic steps can be carried out under suitable laboratory conditions.
Regarding safety information,(2R)-2-[(tert-butoxycarbonyl)amino]butanoate is a chemical, and some safety measures should be paid attention to when using it. Avoid inhalation, contact with skin and eyes. Appropriate protective equipment such as gloves, goggles and laboratory coats should be worn during operation. In addition, it should be operated in a well-ventilated area to prevent the accumulation of harmful compounds. When stored, it should be kept in a dry, cool place and isolated from other chemicals. If necessary, refer to the relevant safety data sheet or consult a professional for more detailed safety information.
(2R)-2-[(tert-butoxycarbonyl)amino]butanoate is widely used in organic synthesis. It is often used as a reagent for protecting amine groups, I .e., an amino group as a Boc group. This protection prevents the amine group from participating in the reaction and also improves the stability of the compound. In synthetic chemistry, various drugs, additives and functional molecules can be synthesized using (2R)-2-[(tert-butoxycarbonyl)amino]butanoate.
The method for preparing (2R)-2-[(tert-butoxycarbonyl)amino]butanoate is usually obtained by reacting 2-aminobutyric acid with tert-butyl carbonate for esterification. The specific synthetic steps can be carried out under suitable laboratory conditions.
Regarding safety information,(2R)-2-[(tert-butoxycarbonyl)amino]butanoate is a chemical, and some safety measures should be paid attention to when using it. Avoid inhalation, contact with skin and eyes. Appropriate protective equipment such as gloves, goggles and laboratory coats should be worn during operation. In addition, it should be operated in a well-ventilated area to prevent the accumulation of harmful compounds. When stored, it should be kept in a dry, cool place and isolated from other chemicals. If necessary, refer to the relevant safety data sheet or consult a professional for more detailed safety information.
Last Update：2024-04-09 20:52:54
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View History
N-boc-dl-2-氨基丁酸
1-[4-[2-Dimethylamino)ethoxy]phenyl]-2-phenyl-1-butanone Hydrochloride
左旋沙丁胺醇相关杂质E(盐酸盐)
2-乙基-4-嘧啶甲醛
5-三氟甲基吡啶-3-羧酸3-羧基-5-三氟甲基吡啶
(1R-cis)-4,6,6-Trimethylbicyclo(3.1.1)hept-3-ene-2-one
N-(2,3-DIOLEOYLOXY-1-PROPYL)TRIMETHYLAMMONIUM METHYL SULFATE
11-MERCAPTOUNDECANOIC ACID
乙酸钠茶碱
Acetazolamide EP Impurity F (Dimer Impurity)
1-[4-[2-Dimethylamino)ethoxy]phenyl]-2-phenyl-1-butanone Hydrochloride
左旋沙丁胺醇相关杂质E(盐酸盐)
2-乙基-4-嘧啶甲醛
5-三氟甲基吡啶-3-羧酸3-羧基-5-三氟甲基吡啶
(1R-cis)-4,6,6-Trimethylbicyclo(3.1.1)hept-3-ene-2-one
N-(2,3-DIOLEOYLOXY-1-PROPYL)TRIMETHYLAMMONIUM METHYL SULFATE
11-MERCAPTOUNDECANOIC ACID
乙酸钠茶碱
Acetazolamide EP Impurity F (Dimer Impurity)