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3-Fluorophenylacetic acid, 98%, Thermo Scientific Chemicals
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Catalog number A15635.14
also known as A15635-14
Price (USD)/ Each
178.00
-
Quantity:
25 g
Price (USD)/ Each
178.00
3-Fluorophenylacetic acid, 98%, Thermo Scientific Chemicals
Catalog numberA15635.14
Price (USD)/ Each
178.00
-
Chemical Identifiers
CAS331-25-9
Specifications
Specification Sheet
Specification SheetAppearance (Color)White to pale cream
FormCrystals or powder or crystalline powder or fused solid or flakes
Assay (Aqueous acid-base Titration)≥97.5 to ≤102.5%
Assay (Silylated GC)≥97.5%
Water Content (Karl Fischer Titration)≤1.5%
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3-Fluorophenylacetic acid has been used as building block to synthesize the pentaamine and bis-heterocyclic libraries. It is also used as a medicine intermediates.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
3-Fluorophenylacetic acid has been used as building block to synthesize the pentaamine and bis-heterocyclic libraries. It is also used as a medicine intermediates.
Solubility
Slightly soluble in chloroform and methanol. Insoluble in water.
Notes
Store at room temperature. Store in cool dry place in tightly closed container. Store away from oxidizing agent.
3-Fluorophenylacetic acid has been used as building block to synthesize the pentaamine and bis-heterocyclic libraries. It is also used as a medicine intermediates.
Solubility
Slightly soluble in chloroform and methanol. Insoluble in water.
Notes
Store at room temperature. Store in cool dry place in tightly closed container. Store away from oxidizing agent.
RUO – Research Use Only
General References:
- Adel Nefzi; Jon Appel; Sergey Arutyunyan; Richard A Houghten; Adel Nefzi; Jon Appel; Sergey Arutyunyan; Richard A. Houghten. Parallel synthesis of chiral pentaamines and pyrrolidine containing bis-heterocyclic libraries. Multiple scaffolds with multiple building blocks: A double diversity for the identification of new antitubercular compounds. Bioorganic & Medicinal Chemistry Letters. 2009, 19 (17), 5169-5175.
- Marisa Cabeza; Eugene Bratoeff; Georgina Gómez; Ivonne Heuze; Arely Rojas; Martha Ochoa; Miguel Angel Palomino; Cristina Revilla. Synthesis and biological effect of halogen substituted phenyl acetic acid derivatives of progesterone as potent progesterone receptor antagonists. The Journal of Steroid Biochemistry and Molecular Biology. 2008, 111 (3-5), 232-239.