2-Hydrazono-3-methyl-2,3-dihydrobenzo[d]thiazolehydrochloride
98%
- Product Code: 118129
Alias:
Related CAS numbers: 1128-67-2 (anhydrous) 149022-15-1 (hydrochloride hydrate); 38894-11-0 (hydrochloride monohydrate); 3-Methyl-2-benzothiazolinone hydrazone HCI
CAS:
14448-67-0
Properties:
Soluble in water, slightly soluble in absolute alcohol
| Molecular Weight: | 215.7 g./mol | Molecular Formula: | C₈H₁₀ClN₃S |
|---|---|---|---|
| EC Number: | 238-428-7 | MDL Number: | |
| Melting Point: | 276-278℃（分解） | Boiling Point: | 369.6ºC at 760 mmHg |
| Density: | Storage Condition: | Room temperature, dry, sealed |
Product Description:
Used as an intermediate in the synthesis of various pharmaceutical compounds, particularly in the development of drugs targeting neurological disorders. It plays a role in the production of compounds with potential anti-inflammatory and antioxidant properties. Additionally, it is utilized in research for creating novel heterocyclic compounds, which are significant in medicinal chemistry for their diverse biological activities. Its application extends to the study of chemical reactions involving hydrazone derivatives, contributing to advancements in organic synthesis methodologies.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | Solid |
| Purity (%) | 97.5-100 |
| Infrared Spectrum | Conforms To Structure |
| Water Content (%) | 2 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿480.00 |
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| 1.000 | 10-20 days | ฿1,320.00 |
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2-Hydrazono-3-methyl-2,3-dihydrobenzo[d]thiazolehydrochloride
Used as an intermediate in the synthesis of various pharmaceutical compounds, particularly in the development of drugs targeting neurological disorders. It plays a role in the production of compounds with potential anti-inflammatory and antioxidant properties. Additionally, it is utilized in research for creating novel heterocyclic compounds, which are significant in medicinal chemistry for their diverse biological activities. Its application extends to the study of chemical reactions involving hydrazone derivatives, contributing to advancements in organic synthesis methodologies.
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