51077-16-8
N-Boc-(R)-thiazolidine-4-carboxylic acid
CAS: 51077-16-8
Molecular Formula: C9H15NO4S
51077-16-8 - Names and Identifiers
51077-16-8 - Physico-chemical Properties
| Molecular Formula | C9H15NO4S |
| Molar Mass | 233.28 |
| Density | 1.305±0.06 g/cm3(Predicted) |
| Melting Point | 125-131°C |
| Boling Point | 385.3±42.0 °C(Predicted) |
| Flash Point | 190.704°C |
| Water Solubility | Insoluble in water. |
| Vapor Presure | 0mmHg at 25°C |
| BRN | 6686084 |
| pKa | 3.53±0.20(Predicted) |
| Storage Condition | Sealed in dry,Room Temperature |
| Refractive Index | 1.525 |
| MDL | MFCD00077002 |
51077-16-8 - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Safety Description | S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. |
| WGK Germany | 3 |
| HS Code | 29341000 |
| Hazard Class | IRRITANT |
51077-16-8 - Introduction
N-Boc-(R)-thiazolidine-4-carboxylic acid is an organic compound whose chemical name is N-Boc-(R)-thiazolidine-4-carboxylic acid. The following is a description of its nature, use, formulation and safety information:
Nature:
N-Boc-(R)-thiazolidine-4-carboxylic acid is a white to yellow solid with a distinctive odor. It is relatively stable at room temperature and soluble in some organic solvents, such as dimethyl sulfoxide and dichloromethane. Its chemical structure contains a thiazole ring and a carboxylic acid functional group.
Use:
N-Boc-(R)-thiazolidine-4-carboxylic acid is a common intermediate compound in organic synthesis. It can be used to synthesize biologically active compounds, such as drugs and pesticides. Its thiazole ring structure makes it have the ability to open the ring reaction and chemical reaction with other functional groups, so it has a wide range of applications in the field of pharmaceutical research and organic synthesis.
Preparation Method:
The preparation of N-Boc-(R)-thiazolidine-4-carboxylic acid is generally carried out by the following steps: First, N-Boc-(R)-cysteine (N-Boc-(R)-cysteine) is reacted with an acid to form N-Boc-(R)-thiazolidine-4-carboxylic acid. The specific reaction conditions can be adjusted according to the specific situation.
Safety Information:
N-Boc-(R)-thiazolidine-4-carboxylic acid is relatively safe in proper use and storage. However, it may have an irritating effect on the eyes and skin, so direct contact should be avoided when using it. At the same time, the operation should follow the appropriate laboratory safety procedures, and be equipped with appropriate personal protective equipment, such as laboratory gloves and protective glasses.
Nature:
N-Boc-(R)-thiazolidine-4-carboxylic acid is a white to yellow solid with a distinctive odor. It is relatively stable at room temperature and soluble in some organic solvents, such as dimethyl sulfoxide and dichloromethane. Its chemical structure contains a thiazole ring and a carboxylic acid functional group.
Use:
N-Boc-(R)-thiazolidine-4-carboxylic acid is a common intermediate compound in organic synthesis. It can be used to synthesize biologically active compounds, such as drugs and pesticides. Its thiazole ring structure makes it have the ability to open the ring reaction and chemical reaction with other functional groups, so it has a wide range of applications in the field of pharmaceutical research and organic synthesis.
Preparation Method:
The preparation of N-Boc-(R)-thiazolidine-4-carboxylic acid is generally carried out by the following steps: First, N-Boc-(R)-cysteine (N-Boc-(R)-cysteine) is reacted with an acid to form N-Boc-(R)-thiazolidine-4-carboxylic acid. The specific reaction conditions can be adjusted according to the specific situation.
Safety Information:
N-Boc-(R)-thiazolidine-4-carboxylic acid is relatively safe in proper use and storage. However, it may have an irritating effect on the eyes and skin, so direct contact should be avoided when using it. At the same time, the operation should follow the appropriate laboratory safety procedures, and be equipped with appropriate personal protective equipment, such as laboratory gloves and protective glasses.
Last Update：2024-04-09 21:11:58
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Email: Int06@meryer.com
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View History
51077-16-8
对三氟甲氧基溴代苯乙酮
M-BROMOFLUOROBENZENE
Diisooctyldithiophosphinic
1,1-dichloroacetone
吲哚菁绿-琥珀酰亚胺酯
二乙基甲基乙烯基硅烷
对三氟甲氧基溴代苯乙酮
M-BROMOFLUOROBENZENE
Diisooctyldithiophosphinic
1,1-dichloroacetone
吲哚菁绿-琥珀酰亚胺酯
二乙基甲基乙烯基硅烷