2-Methyl-2-propanyl [(2S)-2-amino-2-phenylethyl]carbamate
N-[(S)-2-Amino-2-phenylethyl]carbamic acid tert-butyl ester
CAS: 943322-87-0
Molecular Formula: C13H20N2O2
2-Methyl-2-propanyl [(2S)-2-amino-2-phenylethyl]carbamate - Names and Identifiers
2-Methyl-2-propanyl [(2S)-2-amino-2-phenylethyl]carbamate - Physico-chemical Properties
| Molecular Formula | C13H20N2O2 |
| Molar Mass | 236.31 |
| Storage Condition | Keep in dark place,Inert atmosphere,Store in freezer, under -20°C |
2-Methyl-2-propanyl [(2S)-2-amino-2-phenylethyl]carbamate - Introduction
N-[(S)-2-Amino-2-phenylethyl]carbamic acid tert-butyl ester, also known as N-[(S)-2-Amino-2-phenylethyl]carbamic acid tert-butyl ester, is a chemical compound.
Nature:
N-[(S)-2-Amino-2-phenylethyl]carbamic acid tert-butyl ester has a molecular formula of C15H22N2O2 and a relative molecular mass of 262.35. It is a solid and has a scent of benzene. Its melting point is about 102-104°C. This compound is a white or white-like crystal, soluble in some organic solvents.
Use:
N-[(S)-2-Amino-2-phenylethyl]carbamic acid tert-butyl ester is used as an advanced organic synthesis intermediate in the chemical industry. It can be used to synthesize various drugs, pesticides and specific organic compounds. Due to its optical activity, it is also used as a chiral recognition reagent in pharmaceutical research.
Method:
N-[(S)-2-Amino-2-phenylethyl]carbamic acid tert-butyl ester can be obtained by reacting (S)-2-amino -2-phenyl-ethanol with tert-butyl carbamate. Specific steps include an acylation reaction and a substitution reaction. This process needs to be carried out at the appropriate temperature and conditions and with the use of a suitable catalyst.
Safety Information:
N-[(S)-2-Amino-2-phenylethyl]carbamic acid tert-butyl ester has limited safety information. Due to the lack of sufficient toxicological data, detailed information on its potential danger is unclear. Therefore, when using or handling this compound, follow appropriate safety measures, including wearing appropriate protective equipment, ensuring good ventilation, and avoiding contact with skin, eyes, and respiratory tract. If necessary, refer to the relevant safety data sheets and operating instructions to ensure safe use.
Nature:
N-[(S)-2-Amino-2-phenylethyl]carbamic acid tert-butyl ester has a molecular formula of C15H22N2O2 and a relative molecular mass of 262.35. It is a solid and has a scent of benzene. Its melting point is about 102-104°C. This compound is a white or white-like crystal, soluble in some organic solvents.
Use:
N-[(S)-2-Amino-2-phenylethyl]carbamic acid tert-butyl ester is used as an advanced organic synthesis intermediate in the chemical industry. It can be used to synthesize various drugs, pesticides and specific organic compounds. Due to its optical activity, it is also used as a chiral recognition reagent in pharmaceutical research.
Method:
N-[(S)-2-Amino-2-phenylethyl]carbamic acid tert-butyl ester can be obtained by reacting (S)-2-amino -2-phenyl-ethanol with tert-butyl carbamate. Specific steps include an acylation reaction and a substitution reaction. This process needs to be carried out at the appropriate temperature and conditions and with the use of a suitable catalyst.
Safety Information:
N-[(S)-2-Amino-2-phenylethyl]carbamic acid tert-butyl ester has limited safety information. Due to the lack of sufficient toxicological data, detailed information on its potential danger is unclear. Therefore, when using or handling this compound, follow appropriate safety measures, including wearing appropriate protective equipment, ensuring good ventilation, and avoiding contact with skin, eyes, and respiratory tract. If necessary, refer to the relevant safety data sheets and operating instructions to ensure safe use.
Last Update：2024-04-09 21:04:16
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View History
2-Methyl-2-propanyl [(2S)-2-amino-2-phenylethyl]carbamate
6-Hydroxyhexan-6-olide
3-CHLORO-1,1-DIETHOXYPROPANE
Benz[d]indeno[4,5-b]pyran (8CI,9CI)
3-Amino-2-fluorotoluene, 2-Fluoro-m-toluidine
5-Pyrimidinecarboxylic acid, 2-amino-4-hydroxy-6-methyl- (6CI,8CI)
subericaciddinitrile
3-Pyrrolidinecarboxylic acid, 1-methyl-, 1,1-dimethylethyl ester
L(+)-2,3-Diaminopropionic acid hydrochloride
2-methyl-4-chloro-5-hydroxy-6-aminopyrimidine
6-Hydroxyhexan-6-olide
3-CHLORO-1,1-DIETHOXYPROPANE
Benz[d]indeno[4,5-b]pyran (8CI,9CI)
3-Amino-2-fluorotoluene, 2-Fluoro-m-toluidine
5-Pyrimidinecarboxylic acid, 2-amino-4-hydroxy-6-methyl- (6CI,8CI)
subericaciddinitrile
3-Pyrrolidinecarboxylic acid, 1-methyl-, 1,1-dimethylethyl ester
L(+)-2,3-Diaminopropionic acid hydrochloride
2-methyl-4-chloro-5-hydroxy-6-aminopyrimidine