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Home  > 5-Fluoro-6-methyl-1,3-benzothiazol-2-amine

AE28708

1155287-47-0 | 5-Fluoro-6-methyl-1,3-benzothiazol-2-amine

Packsize Purity Availability Price Discounted Price    Quantity
50mg 95% 1 week $250.00 $175.00 -   +
100mg 95% 1 week $332.00 $233.00 -   +
250mg 95% 1 week $441.00 $309.00 -   +
500mg 95% 1 week $646.00 $453.00 -   +
1g 95% 1 week $806.00 $564.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AE28708
Chemical Name: 5-Fluoro-6-methyl-1,3-benzothiazol-2-amine
CAS Number: 1155287-47-0
Molecular Formula: C8H7FN2S
Molecular Weight: 182.218
MDL Number: MFCD08669847
SMILES: Nc1sc2c(n1)cc(c(c2)C)F

 

Upstream Synthesis Route
  • 5-Fluoro-6-methyl-benzothiazol-2-ylamine, also known as $name$, is a versatile compound widely utilized in chemical synthesis. As a key building block in organic chemistry, this compound plays a crucial role in the creation of various pharmaceuticals, agrochemicals, and materials. Its unique structure and reactivity make it an essential component in the development of new molecules with diverse properties and applications.In chemical synthesis, $name$ serves as a valuable intermediate for the production of heterocyclic compounds, which are vital for drug discovery and development. Its incorporation into complex molecular structures enables the synthesis of novel compounds with enhanced biological activities and targeted functionalities. By acting as a precursor in multistep reactions, $name$ facilitates the construction of intricate molecular frameworks, allowing researchers to access a wide range of potential products.Furthermore, the presence of the fluorine and methyl substituents in $name$ imparts specific properties to the resulting compounds, such as increased stability, altered solubility, and enhanced bioavailability. These characteristics make $name$ a favored starting material in the design and synthesis of molecular probes, drug candidates, and specialty chemicals. Its versatility and compatibility with various synthetic methodologies make it a valuable asset in the toolkit of organic chemists seeking to explore new avenues in chemical synthesis.
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