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3-Phenoxyaniline, 98%, Thermo Scientific Chemicals
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Catalog number A17495.06
also known as A17495-06
Price (USD)/ Each
44.40
-
Quantity:
5 g
Price (USD)/ Each
44.40
3-Phenoxyaniline, 98%, Thermo Scientific Chemicals
Catalog numberA17495.06
Price (USD)/ Each
44.40
-
Chemical Identifiers
CAS3586-12-7
IUPAC Name3-phenoxyaniline
Molecular FormulaC12H11NO
InChI KeyUCSYVYFGMFODMY-UHFFFAOYSA-N
SMILESNC1=CC=CC(OC2=CC=CC=C2)=C1
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Specifications
Specification Sheet
Specification SheetAppearance (Color)White to cream or pale yellow to pale brown
FormCrystals or powder or crystalline powder or fused solid
Assay (GC)≥97.5%
Melting Point (clear melt)32.0-40.0°C
3-Phenoxyaniline was used in the preparation of 4-phenoxyaniline-3?-bromopropionamide. It is also used in the design, synthesis and evaluation of potential inhibitors of HIV gp120-CD4 interactions.
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-Phenoxyaniline was used in the preparation of 4-phenoxyaniline-3′-bromopropionamide. It is also used in the design, synthesis and evaluation of potential inhibitors of HIV gp120-CD4 interactions.
Solubility
Slightly soluble in water.
Notes
Store away from oxidizing agents. Keep the container tightly closed and place it in a cool, dry and well ventilated condition.
3-Phenoxyaniline was used in the preparation of 4-phenoxyaniline-3′-bromopropionamide. It is also used in the design, synthesis and evaluation of potential inhibitors of HIV gp120-CD4 interactions.
Solubility
Slightly soluble in water.
Notes
Store away from oxidizing agents. Keep the container tightly closed and place it in a cool, dry and well ventilated condition.
RUO – Research Use Only
General References:
- Dona Chianelli, et al. Application of a novel design paradigm to generate general nonpeptide combinatorial scaffolds mimicking beta turns: synthesis of ligands for somatostatin receptors.Bioorg Med Chem.,2003,11(23), 5059-5068.
- Mark A. Massa. Novel heteroaryl replacements of aromatic 3-tetrafluoroethoxy substituents in trifluoro-3-(tertiaryamino)-2-propanols as potent inhibitors of cholesteryl ester transfer protein.Bioorg. Med. Chem. Lett.,2001,11(13), 1625-1628.