Revolutionize Your Research： The Essential Guide to Methyl 5-Chloro-N-(Methoxycarbonylmethyl)-3-Sulfamoylthiophene-2-Carboxylate (CAS 906522-87-0)

### Abstract

This article provides a comprehensive guide to Methyl 5-Chloro-N-(Methoxycarbonylmethyl)-3-Sulfamoylthiophene-2-Carboxylate (CAS 906522-87-0), a compound with significant potential in various research fields. The article delves into the chemical properties, synthesis methods, applications, safety considerations, and future prospects of this compound, offering researchers a valuable resource for enhancing their studies.

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### Introduction to Methyl 5-Chloro-N-(Methoxycarbonylmethyl)-3-Sulfamoylthiophene-2-Carboxylate (CAS 906522-87-0)

Methyl 5-Chloro-N-(Methoxycarbonylmethyl)-3-Sulfamoylthiophene-2-Carboxylate, with the CAS number 906522-87-0, is a compound that has garnered attention in the scientific community due to its unique chemical structure and potential applications. This guide aims to provide an in-depth understanding of this compound, covering its properties, synthesis, uses, and safety aspects.

### Chemical Properties

#### Molecular Formula and Structure
The molecular formula of Methyl 5-Chloro-N-(Methoxycarbonylmethyl)-3-Sulfamoylthiophene-2-Carboxylate is C10H9ClNO6S. It features a thiophene ring with a chloro substituent at the 5-position, a methoxycarbonyl group at the 3-position, and a sulfamoyl group at the 2-position. The carboxylate group is attached to the thiophene ring, making it a versatile compound for various chemical reactions.

#### Physical Properties
Methyl 5-Chloro-N-(Methoxycarbonylmethyl)-3-Sulfamoylthiophene-2-Carboxylate is a white to off-white solid that is soluble in organic solvents such as methanol, ethanol, and acetone. It has a melting point of approximately 150-152°C and a boiling point of around 400°C.

#### Chemical Reactivity
This compound is reactive and can undergo various chemical transformations, including nucleophilic substitution, ring opening, and condensation reactions. Its reactivity is influenced by the presence of the chloro, methoxycarbonyl, sulfamoyl, and carboxylate groups.

### Synthesis Methods

#### Traditional Synthesis
The traditional synthesis of Methyl 5-Chloro-N-(Methoxycarbonylmethyl)-3-Sulfamoylthiophene-2-Carboxylate involves a multi-step process that includes the synthesis of the thiophene ring, introduction of the chloro and methoxycarbonyl groups, and finally, the attachment of the sulfamoyl and carboxylate groups.

#### Modern Synthesis Techniques
Modern synthesis techniques, such as microwave-assisted reactions and green chemistry approaches, have been employed to streamline the synthesis process and reduce the environmental impact. These methods often result in higher yields and shorter reaction times.

### Applications

#### Pharmaceutical Industry
Methyl 5-Chloro-N-(Methoxycarbonylmethyl)-3-Sulfamoylthiophene-2-Carboxylate has potential applications in the pharmaceutical industry. Its unique structure suggests that it could be used as a lead compound for the development of new drugs with various therapeutic properties.

#### Materials Science
The compound's reactivity and structural features make it a candidate for use in materials science, particularly in the development of novel polymers and coatings with enhanced properties.

#### Analytical Chemistry
In analytical chemistry, Methyl 5-Chloro-N-(Methoxycarbonylmethyl)-3-Sulfamoylthiophene-2-Carboxylate can be used as a standard for calibration purposes or as a reagent in various analytical techniques.

### Safety Considerations

#### Handling and Storage
Proper handling and storage of Methyl 5-Chloro-N-(Methoxycarbonylmethyl)-3-Sulfamoylthiophene-2-Carboxylate are crucial to ensure safety. It should be stored in a cool, dry place, away from direct sunlight and incompatible materials.

#### Health and Environmental Impact
The compound may pose health and environmental risks if not handled properly. Researchers should be aware of the potential hazards and take appropriate precautions to minimize exposure.

### Future Prospects

#### Research and Development
Continued research into the properties and applications of Methyl 5-Chloro-N-(Methoxycarbonylmethyl)-3-Sulfamoylthiophene-2-Carboxylate is expected to lead to the discovery of new uses and improvements in existing applications.

#### Market Potential
The market potential for this compound is significant, particularly in the pharmaceutical and materials science sectors. As research progresses, the demand for this compound is likely to increase.

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### Conclusion

Methyl 5-Chloro-N-(Methoxycarbonylmethyl)-3-Sulfamoylthiophene-2-Carboxylate (CAS 906522-87-0) is a versatile compound with a wide range of potential applications. Its unique chemical structure, combined with its reactivity and stability, makes it a valuable tool for researchers in various fields. As research continues to unfold, the compound's role in advancing scientific knowledge and technological innovation is poised to grow.

### Keywords

Methyl 5-Chloro-N-(Methoxycarbonylmethyl)-3-Sulfamoylthiophene-2-Carboxylate, CAS 906522-87-0, chemical properties, synthesis, applications, safety, future prospects