(5-Methoxycarbonylamino-[1,2,4]Thiadiazol-3-Yl)-Acetic Acid Methyl Ester
(5-Methoxycarbonylamino-[1,2,4]Thiadiazol-3-Yl)-Acetic Acid Methyl Ester
CAS: 149196-71-4
Molecular Formula: C7H9N3O4S
(5-Methoxycarbonylamino-[1,2,4]Thiadiazol-3-Yl)-Acetic Acid Methyl Ester - Names and Identifiers
(5-Methoxycarbonylamino-[1,2,4]Thiadiazol-3-Yl)-Acetic Acid Methyl Ester - Physico-chemical Properties
| Molecular Formula | C7H9N3O4S |
| Molar Mass | 231.23 |
(5-Methoxycarbonylamino-[1,2,4]Thiadiazol-3-Yl)-Acetic Acid Methyl Ester - Introduction
(5-methoxy carbonylamino-[1,2,4]Thiadiazol-3-Yl)-Acetic Acid Methyl Ester, also known as MTMST, is an organic compound. The following is a description of the properties, uses, preparation and safety information of the compound:
Nature:
1. Appearance: Colorless to light yellow solid.
2. Molecular formula: C9H10N2O4S.
3. Molecular weight: 238.25g/mol.
4. Melting Point: 70-74 ℃.
5. Boiling point: 395.6 ℃.
6. Solubility: Soluble in alcohol, Ester and ether, slightly soluble in water.
Use:
MTMST is often used as a chemical reagent in organic synthesis. Specific applications include:
1. Catalyst: As a ligand of copper (II) salt, it participates in the catalysis of many organic oxidation reactions.
2. Medium: As an acetate solvent, it plays the role of solvent and protecting group in organic synthesis reaction.
3. Reagent: used for the synthesis of other compounds, such as thiazole mercaptan, thiolate acid ester and sulfate, etc.
Method:
The synthesis of MTMST can be carried out by the following steps:
1. Methylation reaction: methyl acetate is reacted with methyl sulfate to obtain methyl methyl sulfate.
2. Electrophilic substitution reaction: methyl sulfate is reacted with 2-amino -4, 5-dithiopyridine to obtain the target product MTMST.
Safety Information:
1. MTMST is an organic compound with certain toxicity and potential danger.
2. In the operation and storage should pay attention to prevent contact with eyes, skin and taking.
3. Use should wear protective glasses, gloves and protective clothing, and pay attention to a well-ventilated working environment.
4. During use and handling, comply with relevant safety operation regulations, and strictly control the risk of fire and static electricity accumulation.
5. If you take it by mistake or enter your eyes and skin by mistake, you should wash it with plenty of water immediately and seek the advice of your doctor.
Nature:
1. Appearance: Colorless to light yellow solid.
2. Molecular formula: C9H10N2O4S.
3. Molecular weight: 238.25g/mol.
4. Melting Point: 70-74 ℃.
5. Boiling point: 395.6 ℃.
6. Solubility: Soluble in alcohol, Ester and ether, slightly soluble in water.
Use:
MTMST is often used as a chemical reagent in organic synthesis. Specific applications include:
1. Catalyst: As a ligand of copper (II) salt, it participates in the catalysis of many organic oxidation reactions.
2. Medium: As an acetate solvent, it plays the role of solvent and protecting group in organic synthesis reaction.
3. Reagent: used for the synthesis of other compounds, such as thiazole mercaptan, thiolate acid ester and sulfate, etc.
Method:
The synthesis of MTMST can be carried out by the following steps:
1. Methylation reaction: methyl acetate is reacted with methyl sulfate to obtain methyl methyl sulfate.
2. Electrophilic substitution reaction: methyl sulfate is reacted with 2-amino -4, 5-dithiopyridine to obtain the target product MTMST.
Safety Information:
1. MTMST is an organic compound with certain toxicity and potential danger.
2. In the operation and storage should pay attention to prevent contact with eyes, skin and taking.
3. Use should wear protective glasses, gloves and protective clothing, and pay attention to a well-ventilated working environment.
4. During use and handling, comply with relevant safety operation regulations, and strictly control the risk of fire and static electricity accumulation.
5. If you take it by mistake or enter your eyes and skin by mistake, you should wash it with plenty of water immediately and seek the advice of your doctor.
Last Update：2024-04-10 22:29:15
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