(S)-1-(2-Fluorophenyl)Ethanol(CAS 171032-87-4)
| Purity | Grade | Package | Stock | Price | Quantity |
| 99% | RG | 1G | In Stock | 17 USD
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| 99% | RG | 5G | In Stock | 72 USD
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| 99% | RG | 25G | In Stock | 232 USD
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| Bulk Packaging | 1KG | substantially lower unit cost than small-pack SKUs. Contact us for a fast quotation. | |||
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Your region is eligible for ordering. Available NMR Spectrum
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Applications of 171032-87-4
| Industry | Application | Process |
|---|---|---|
| Pharmaceuticals | Used in the synthesis of pharmaceutical intermediates, such as antidepressants and anxiolytics | Prepared via asymmetric synthesis; employed as a chiral intermediate in subsequent condensation or substitution reactions |
| Agrochemicals | Used in the synthesis of agrochemical intermediates, such as insecticides and herbicides | Prepared via fluorination, oxidation, and other processes; serves as a chiral building block in the synthesis of active agrochemical ingredients |
| Fine Fragrances | Used in the synthesis of fragrance compounds, including certain floral notes | Prepared via epoxidation, reduction, and other processes; further applied in structural modification and functionalization of fragrance molecules |
| Solvents | Used as chiral resolution solvents or reaction media | Leverages its chirality as a resolving agent in solvent systems or as a chiral inducer during reactions |
| Cosmetics | Used in the synthesis of certain cosmetic ingredients, such as UV filters or humectants | Employed as a chiral intermediate in esterification or etherification reactions to produce optically active cosmetic ingredients |
| Biotechnology | Used in the synthesis of bioactive molecules, such as certain hormones or enzyme inhibitors | Prepared via enzymatic or chemical asymmetric synthesis; used as a building block in the synthesis of complex molecules |
| Materials Science | Used in the synthesis of chiral materials or polymer intermediates | Applied as a chiral monomer in the synthesis of cyclic or block polymers, or as a chiral catalyst in material synthesis |
| Environmental Science | Used to study the environmental behavior and degradation pathways of chiral compounds | Investigated via isotopic labeling or tracer methods to assess environmental migration, transformation, and degradation patterns, and to evaluate environmental impact |
| Pharmaceutical Intermediates | Used in the synthesis of various chiral pharmaceutical intermediates | Prepared via multiple asymmetric synthesis routes, including enzymatic reduction, chemical asymmetric oxidation, or selective synthesis using chiral catalysts |
Physical and chemical properties of 171032-87-4
Acidity coefficient |
13.95±0.20(Predicted) |
|---|---|
Boiling Point |
193.1±15.0 °C at 760 mmHg |
Density |
1.1±0.1 g/cm3 |
Exact Mass |
140.063736 |
Flash Point |
87.9±7.2 °C |
Index of Refraction |
1.511 |
LogP |
1.43 |
Molecular Formula |
C8H9FO |
Molecular Weight |
140.155 |
PSA |
20.23000 |
Storage condition |
Sealed in dry,Room Temperature |
Vapour Pressure |
0.3±0.4 mmHg at 25°C |
Spectrums of 171032-87-4
1.The NMR spectrum displayed on the page is a pre-sale reference spectrum and may differ from that of the actual received batch.
2.The accompanying documentation will include the NMR spectrum and purity analysis data for the shipped batch.
Retrosynthesis analysis of 171032-87-4
Cas:445-26-1
Cas:445-27-2
Cas:67-63-0
Q&A for CAS 171032-87-4
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Yes. Batch COA available matches the actual shipment. COAs shown online are for reference or from previous batches.
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Download SDS of 171032-87-4
Pictograms |
 |
|---|---|
Signal Word |
Warning |
Hazard Statements |
H302 Harmful if swallowed H315 Causes skin irritation H319 Causes serious eye irritation H335 May cause respiratory irritation |
Safety Data Sheet |
Download COA of 171032-87-4
Operate under the ISO 9001 system
