3-Oxazolidinecarboxylic acid, 4-(hydroxymethyl)-2,2-dimethyl-, 1,1-dimethylethyl ester, (4S)-
(S)-4-Hydroxymethyl-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester
CAS: 108149-65-1
Molecular Formula: C11H21NO4
3-Oxazolidinecarboxylic acid, 4-(hydroxymethyl)-2,2-dimethyl-, 1,1-dimethylethyl ester, (4S)- - Names and Identifiers
3-Oxazolidinecarboxylic acid, 4-(hydroxymethyl)-2,2-dimethyl-, 1,1-dimethylethyl ester, (4S)- - Physico-chemical Properties
| Molecular Formula | C11H21NO4 |
| Molar Mass | 231.29 |
| Density | 1.075±0.06 g/cm3(Predicted) |
| Melting Point | 36 °C |
| Boling Point | 314.1±27.0 °C(Predicted) |
| Flash Point | 143.745°C |
| Vapor Presure | 0mmHg at 25°C |
| pKa | 14.54±0.10(Predicted) |
| Storage Condition | 2-8°C |
| Refractive Index | 1.464 |
3-Oxazolidinecarboxylic acid, 4-(hydroxymethyl)-2,2-dimethyl-, 1,1-dimethylethyl ester, (4S)- - Introduction
(S)-tert-butyl 4-hydroxymethyl-2, 2-dimethyloxazolidine-3-carboxylate is an organic compound. The following is a description of its nature, use, formulation and safety information:
Nature:
(S)-tert-butyl 4-hydroxymethyl-2, 2-dimethyloxazolidine-3-carboxylate is a colorless to pale yellow clear liquid. It has low volatility and relatively high stability at room temperature. The compounds have low solubility and are soluble in organic solvents such as ethers and esters.
Use:
The compound has important application value in the field of organic synthesis. As a chiral reagent, it is often used to catalyze asymmetric synthesis reactions for the preparation of chiral compounds. In addition, it can also be used as an intermediate for some drugs, such as lead compounds for the synthesis of some chiral drugs.
Preparation Method:
The preparation method of (S)-4-hydroxymethyl-2, 2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester is usually obtained by reacting the corresponding acid chloride with (S)-(-)-2,2-dimethyloxazolidine-3-methanol.
Safety Information:
This is a chemical, the operator should pay attention to safety. It may cause irritation to the eyes and skin and may cause damage to the respiratory system. During use, contact with skin and eyes should be avoided, and protective glasses and gloves should be worn if necessary. At the same time, it should be used in a well-ventilated place and avoid inhaling its gas or vapor. In case of inhalation or skin contact, rinse immediately with water and seek medical attention.
Nature:
(S)-tert-butyl 4-hydroxymethyl-2, 2-dimethyloxazolidine-3-carboxylate is a colorless to pale yellow clear liquid. It has low volatility and relatively high stability at room temperature. The compounds have low solubility and are soluble in organic solvents such as ethers and esters.
Use:
The compound has important application value in the field of organic synthesis. As a chiral reagent, it is often used to catalyze asymmetric synthesis reactions for the preparation of chiral compounds. In addition, it can also be used as an intermediate for some drugs, such as lead compounds for the synthesis of some chiral drugs.
Preparation Method:
The preparation method of (S)-4-hydroxymethyl-2, 2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester is usually obtained by reacting the corresponding acid chloride with (S)-(-)-2,2-dimethyloxazolidine-3-methanol.
Safety Information:
This is a chemical, the operator should pay attention to safety. It may cause irritation to the eyes and skin and may cause damage to the respiratory system. During use, contact with skin and eyes should be avoided, and protective glasses and gloves should be worn if necessary. At the same time, it should be used in a well-ventilated place and avoid inhaling its gas or vapor. In case of inhalation or skin contact, rinse immediately with water and seek medical attention.
Last Update：2024-04-09 21:11:58
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Product Name: (S)-tert-Butyl 4-(hydroxymethyl)-2,2-dimethyloxazolidine-3-carboxylate Visit Supplier Webpage Request for quotationCAS: 108149-65-1
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CAS: 108149-65-1
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CAS: 108149-65-1
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View History
3-Oxazolidinecarboxylic acid, 4-(hydroxymethyl)-2,2-dimethyl-, 1,1-dimethylethyl ester, (4S)-
2-(氰基甲基)苯甲酸甲酯
(2Z)-3-(4-chlorophenyl)-1-[3-(trifluoromethyl)phenyl]prop-2-en-1-one
3-(4-NITROPHENYL)-3-OXOPROPANENITRILE
3H-Imidazo[4,5-b]pyridin-7-amine, 5-methyl-
2-(氰基甲基)苯甲酸甲酯
(2Z)-3-(4-chlorophenyl)-1-[3-(trifluoromethyl)phenyl]prop-2-en-1-one
3-(4-NITROPHENYL)-3-OXOPROPANENITRILE
3H-Imidazo[4,5-b]pyridin-7-amine, 5-methyl-