2-AMINO-6-IODOBENZOTHIAZOLE
97%
- Product Code: 116357
CAS:
16582-58-4
| Molecular Weight: | 276.096 g./mol | Molecular Formula: | C₇H₅IN₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00996639 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
2-Amino-6-iodobenzothiazole is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex chemical compounds. Its structure, featuring both amino and iodo functional groups, makes it a valuable building block in the synthesis of heterocyclic compounds, which are often explored for their potential pharmaceutical applications. This compound is particularly significant in the preparation of benzothiazole derivatives, which are studied for their biological activities, including antimicrobial, anticancer, and anti-inflammatory properties. Additionally, it serves as a precursor in the synthesis of fluorescent dyes and imaging agents, contributing to advancements in diagnostic and research tools. Its role in the development of materials for optoelectronic devices is also noteworthy, as benzothiazole derivatives are investigated for their electronic and photophysical properties.
Product Specification:
| Test | Specification |
|---|---|
| Purity (%) | 97-100 |
| Appearance | Solid |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿4,800.00 |
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| 1.000 | 10-20 days | ฿18,920.00 |
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2-AMINO-6-IODOBENZOTHIAZOLE
2-Amino-6-iodobenzothiazole is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex chemical compounds. Its structure, featuring both amino and iodo functional groups, makes it a valuable building block in the synthesis of heterocyclic compounds, which are often explored for their potential pharmaceutical applications. This compound is particularly significant in the preparation of benzothiazole derivatives, which are studied for their biological activities, including antimicrobial, anticancer, and anti-inflammatory properties. Additionally, it serves as a precursor in the synthesis of fluorescent dyes and imaging agents, contributing to advancements in diagnostic and research tools. Its role in the development of materials for optoelectronic devices is also noteworthy, as benzothiazole derivatives are investigated for their electronic and photophysical properties.
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