N-[(2R)-1-hydroxypropan-2-yl]carbamic acid (phenylmethyl) ester
Z-D-Alaninol
CAS: 61425-27-2
Molecular Formula: C11H15NO3
N-[(2R)-1-hydroxypropan-2-yl]carbamic acid (phenylmethyl) ester - Names and Identifiers
| Name | Z-D-Alaninol |
| Synonyms | Z-D-Alaninol Cbz-D-Alaninol N-Z-D-Alaninol N-Z-D-ALANINOL N-CBZ-D-ALANINOL N-Benzyloxycarbony L-D-Alaninoln-Cbz-D-Alaninol (R)-2-(Cbz-amino)-1-propanol N-Benzyloxycarbonyl-D-Alaninol N-BENZYLOXYCARBONYL-D-ALANINOL (R)-(+)-2-(Z-AMINO)-1-PROPANOL (R)-(+)-2-(Z-Amino)-1-Propanol Benzyl (R)-(1-hydroxypropan-2-yl)carbamate benzyl N-[(2R)-1-hydroxypropan-2-yl]carbamate benzyl [(1R)-2-hydroxy-1-methylethyl]carbamate N-[(2R)-1-hydroxypropan-2-yl]carbamic acid (phenylmethyl) ester |
| CAS | 61425-27-2 |
| EINECS | 1533716-785-6 |
| InChI | InChI=1/C11H15NO3/c1-9(7-13)12-11(14)15-8-10-5-3-2-4-6-10/h2-6,9,13H,7-8H2,1H3,(H,12,14)/t9-/m1/s1 |
N-[(2R)-1-hydroxypropan-2-yl]carbamic acid (phenylmethyl) ester - Physico-chemical Properties
| Molecular Formula | C11H15NO3 |
| Molar Mass | 209.24 |
| Density | 1.149±0.06 g/cm3(Predicted) |
| Melting Point | 82-84°C |
| Boling Point | 375.2±35.0 °C(Predicted) |
| Flash Point | 180.7°C |
| Vapor Presure | 2.7E-06mmHg at 25°C |
| pKa | 11.90±0.46(Predicted) |
| Storage Condition | 2-8°C |
| Refractive Index | 1.534 |
| MDL | MFCD00672531 |
| Physical and Chemical Properties | Storage method: 2-10 ℃ |
N-[(2R)-1-hydroxypropan-2-yl]carbamic acid (phenylmethyl) ester - Risk and Safety
| Safety Description | 24/25 - Avoid contact with skin and eyes. |
| WGK Germany | 3 |
| HS Code | 29221990 |
N-[(2R)-1-hydroxypropan-2-yl]carbamic acid (phenylmethyl) ester - Introduction
Z-D-Alaninol(Z-D-Alaninol) is an organic compound with the chemical formula C6H13NO2. The following is a description of the nature, use, preparation and safety information of the Z-D-Alaninol:
Nature:
Z-D-Alaninol is a solid with a white to light yellow color. It is a mixture obtained by the reaction of D-alanine with a Z-protecting group (Z = malic acid methyl ester) and can be used as an important intermediate in organic synthesis. It is soluble in water and some organic solvents such as ethanol and dimethylformamide.
Use:
Z-D-Alaninol can be used in a variety of reactions in organic synthesis, commonly used in the synthesis of peptides and proteins. It can act as a protecting group for alanine, protecting the amino function of alanine during the synthesis to avoid its participation in other reactions. Through the protection of Z-D-Alaninol, the structure and function of alanine can be effectively maintained, and the correct position in chemical synthesis can be ensured.
Preparation Method:
The preparation method of Z-D-Alaninol is generally by adding a Z-protecting group (such as malic acid methyl ester) to D-alanine, and then performing the reaction using an appropriate solvent. By adjusting the reaction conditions, such as temperature and reaction time, high purity Z-D-Alaninol can be obtained.
Safety Information:
There are currently no special reports regarding the safety information of the Z-D-Alaninol. However, as organic compounds, direct contact with the skin and eyes should generally be avoided, and care should be taken to avoid inhalation or ingestion. During use, appropriate laboratory practices should be observed and appropriate protective equipment, such as laboratory gloves and goggles, should be worn. In case of accidental contact, please rinse immediately with plenty of water and receive medical treatment in time. During use, be sure to follow the correct chemical waste disposal methods.
Nature:
Z-D-Alaninol is a solid with a white to light yellow color. It is a mixture obtained by the reaction of D-alanine with a Z-protecting group (Z = malic acid methyl ester) and can be used as an important intermediate in organic synthesis. It is soluble in water and some organic solvents such as ethanol and dimethylformamide.
Use:
Z-D-Alaninol can be used in a variety of reactions in organic synthesis, commonly used in the synthesis of peptides and proteins. It can act as a protecting group for alanine, protecting the amino function of alanine during the synthesis to avoid its participation in other reactions. Through the protection of Z-D-Alaninol, the structure and function of alanine can be effectively maintained, and the correct position in chemical synthesis can be ensured.
Preparation Method:
The preparation method of Z-D-Alaninol is generally by adding a Z-protecting group (such as malic acid methyl ester) to D-alanine, and then performing the reaction using an appropriate solvent. By adjusting the reaction conditions, such as temperature and reaction time, high purity Z-D-Alaninol can be obtained.
Safety Information:
There are currently no special reports regarding the safety information of the Z-D-Alaninol. However, as organic compounds, direct contact with the skin and eyes should generally be avoided, and care should be taken to avoid inhalation or ingestion. During use, appropriate laboratory practices should be observed and appropriate protective equipment, such as laboratory gloves and goggles, should be worn. In case of accidental contact, please rinse immediately with plenty of water and receive medical treatment in time. During use, be sure to follow the correct chemical waste disposal methods.
Last Update：2024-04-10 22:29:15
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CAS: 61425-27-2
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Mobile: 18021002903
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