[2-(2-fluorophenyl)-2-oxoethyl]propanedinitrile
98%
- Product Code: 80789
CAS:
312307-38-3
Molecular Weight: | 202.18 g./mol | Molecular Formula: | C₁₁H₇FN₂O |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized in the synthesis of various organic compounds, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring a fluorophenyl group and a dinitrile moiety, makes it a valuable intermediate in the creation of molecules with potential biological activity. It is often employed in the preparation of heterocyclic compounds, which are key components in many drugs targeting neurological and cardiovascular disorders. Additionally, its reactivity allows for its use in the production of specialized dyes and pigments. In research settings, it serves as a building block for exploring novel chemical reactions and pathways, contributing to advancements in synthetic organic chemistry.
Product Specification:
Test | Specification |
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APPEARANCE | Light brown to brown Solid |
PURITY | 97.5-100 |
Infrared spectrum | Conforms to Structure |
NMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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5.000 | 10-20 days | ฿2,350.00 |
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25.000 | 10-20 days | ฿6,840.00 |
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100.000 | 10-20 days | ฿24,860.00 |
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[2-(2-fluorophenyl)-2-oxoethyl]propanedinitrile
This chemical is primarily utilized in the synthesis of various organic compounds, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring a fluorophenyl group and a dinitrile moiety, makes it a valuable intermediate in the creation of molecules with potential biological activity. It is often employed in the preparation of heterocyclic compounds, which are key components in many drugs targeting neurological and cardiovascular disorders. Additionally, its reactivity allows for its use in the production of specialized dyes and pigments. In research settings, it serves as a building block for exploring novel chemical reactions and pathways, contributing to advancements in synthetic organic chemistry.
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