N-cbz-O-T-butyl-L-serine
N-Z-O-tert-butyl-L-serine
CAS: 1676-75-1
Molecular Formula: C15H21NO5
N-cbz-O-T-butyl-L-serine - Names and Identifiers
| Name | N-Z-O-tert-butyl-L-serine |
| Synonyms | Z-Ser(tBu)-OH Z-Ser(But)-OH Z-L-SER(TBU)-OH Z-O-T-BUTYL-L-SERINE Carbobenzoxybutylserine Z-O-tert.butyl-L-serine N-cbz-O-T-butyl-L-serine N-Z-O-tert-butyl-L-serine N-Z-O-TERT-BUTYL-L-SERINE N-Cbz-O-tert-butyl-L-serine N-CBZ-O-TERT-BUTYL-L-SERINE N-ALPHA-CBZ-O-T-BUTYL-L-SERINE N-Carbobenzoxy-O-tert-butyl-L-serine N-CARBOBENZOXY-O-TERT-BUTYL-L-SERINE N-ALPHA-CARBOBENZOXY-O-T-BUTYL L-SERINE N-[(benzyloxy)carbonyl]-O-tert-butylserine N-[(benzyloxy)carbonyl]-O-tert-butyl-L-serine N-[(benzyloxy)carbonyl]-O-tert-butyl-D-serine N-ALPHA-BENZYLOXYCARBONYL-O-TERT-BUTYL-L-SERINE |
| CAS | 1676-75-1 |
| EINECS | 216-827-7 |
| InChI | InChI=1/C15H21NO5/c1-15(2,3)21-10-12(13(17)18)16-14(19)20-9-11-7-5-4-6-8-11/h4-8,12H,9-10H2,1-3H3,(H,16,19)(H,17,18)/t12-/m1/s1 |
| InChIKey | TXDGEONUWGOCJG-LBPRGKRZSA-N |
N-cbz-O-T-butyl-L-serine - Physico-chemical Properties
| Molecular Formula | C15H21NO5 |
| Molar Mass | 295.33 |
| Density | 1.174±0.06 g/cm3(Predicted) |
| Melting Point | 148 °C |
| Boling Point | 465.3±45.0 °C(Predicted) |
| Flash Point | 235.2°C |
| Vapor Presure | 1.85E-09mmHg at 25°C |
| BRN | 2000284 |
| pKa | 3.54±0.10(Predicted) |
| Storage Condition | Sealed in dry,2-8°C |
| Refractive Index | 20.5 ° (C=1, EtOH) |
| MDL | MFCD00038275 |
N-cbz-O-T-butyl-L-serine - Risk and Safety
| WGK Germany | 3 |
| HS Code | 29242990 |
N-cbz-O-T-butyl-L-serine - Introduction
N-Z-O-tert-butyl-L-serine is an organic compound with the chemical formula C14H21NO5. The following is a description of its nature, use, preparation and safety information:
Nature:
N-Z-O-tert-butyl-L-serine is a white crystalline solid. Its melting point is about 120-130 degrees Celsius. It is slightly soluble in water and more soluble in organic solvents. It is an unstable compound and easily degraded.
Use:
N-Z-O-tert-butyl-L-serine is usually used as an intermediate in chemical synthesis reactions. It can be used to synthesize antibiotics, drugs and other organic compounds.
Method:
N-Z-O-tert-butyl-L-serine can be obtained by a variety of synthetic methods. A common method of preparation is the reaction of tert-butyl L-serine with benzyl carbonate under basic conditions to give the target compound.
Safety Information:
The use of N-Z-O-tert-butyl-L-serine is subject to the safe practice of chemical laboratories. It may cause irritation and damage to the eyes, skin and respiratory tract, so it is necessary to wear appropriate personal protective equipment during operation, such as safety glasses, gloves and protective clothing. In addition, it may also cause harm to the environment, and waste should be handled and disposed of properly.
Nature:
N-Z-O-tert-butyl-L-serine is a white crystalline solid. Its melting point is about 120-130 degrees Celsius. It is slightly soluble in water and more soluble in organic solvents. It is an unstable compound and easily degraded.
Use:
N-Z-O-tert-butyl-L-serine is usually used as an intermediate in chemical synthesis reactions. It can be used to synthesize antibiotics, drugs and other organic compounds.
Method:
N-Z-O-tert-butyl-L-serine can be obtained by a variety of synthetic methods. A common method of preparation is the reaction of tert-butyl L-serine with benzyl carbonate under basic conditions to give the target compound.
Safety Information:
The use of N-Z-O-tert-butyl-L-serine is subject to the safe practice of chemical laboratories. It may cause irritation and damage to the eyes, skin and respiratory tract, so it is necessary to wear appropriate personal protective equipment during operation, such as safety glasses, gloves and protective clothing. In addition, it may also cause harm to the environment, and waste should be handled and disposed of properly.
Last Update：2024-04-09 20:52:54
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View History
N-cbz-O-T-butyl-L-serine
Benzene, 1-broMo-2-chloro-3-Methyl-
N-芴甲氧羰酰基-N-甲基-O-苄基-L-苏氨酸
5,6-二氨基-1-甲基尿嘧啶
3,3,3-Trifluoropropylene
Benzene, 1-broMo-2-chloro-3-Methyl-
N-芴甲氧羰酰基-N-甲基-O-苄基-L-苏氨酸
5,6-二氨基-1-甲基尿嘧啶
3,3,3-Trifluoropropylene