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2-Bromo-4'-methoxyacetophenone, 98%, Thermo Scientific Chemicals
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Catalog number A13415.06
also known as A13415-06
Price (USD)/ Each
39.30
-
Quantity:
5 g
Price (USD)/ Each
39.30
2-Bromo-4'-methoxyacetophenone, 98%, Thermo Scientific Chemicals
Catalog numberA13415.06
Price (USD)/ Each
39.30
-
Chemical Identifiers
CAS2632-13-5
IUPAC Name2-bromo-1-(4-methoxyphenyl)ethan-1-one
Molecular FormulaC9H9BrO2
InChI KeyXQJAHBHCLXUGEP-UHFFFAOYSA-N
SMILESCOC1=CC=C(C=C1)C(=O)CBr
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Specifications
Specification Sheet
Specification SheetFormCrystals or powder or crystalline powder
Identification (FTIR)Conforms
Assay (GC)≥97.5%
Appearance (Color)White to cream to pale brown
Melting Point (clear melt)67-73?C
2-Bromo-4'-methoxyacetophenone, is used as a cell-permeable, covalent and potent protein tyrosine phosphatase inhibitor.
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
2-Bromo-4′-methoxyacetophenone, is used as a cell-permeable, covalent and potent protein tyrosine phosphatase inhibitor.
Solubility
It is soluble in DMSO, water (partly miscible), most organic solvents, and methanol.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Recommended storage temperature: 2 - 8°C
2-Bromo-4′-methoxyacetophenone, is used as a cell-permeable, covalent and potent protein tyrosine phosphatase inhibitor.
Solubility
It is soluble in DMSO, water (partly miscible), most organic solvents, and methanol.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Recommended storage temperature: 2 - 8°C
RUO – Research Use Only
General References:
- W Zhang.; DP Curran.; CHT Chen. Use of fluorous silica gel to separate fluorous thiol quenching derivatives in solution-phase parallel synthesis. Tetrahedron letters. 2002, 58,(20), 3871-3875.
- Y Nishiyama.; A Kobayashi. Synthesis of 1, 4-diketones: reaction of α-bromo ketones with tetrakis (dimethylamino) ethylene (TDAE). Tetrahedron letters. 2006, 47,(31), 5565-5567.
- Reagent for protection of carboxylic acids as 4-methoxyphenacyl esters, which may be prepared in the presence of KF as base: Synthesis, 897 (1981) and can be cleaved photolytically: J. Org. Chem., 38, 3771 (1973). Peptide bonds are generally unaffected by irradiation but some cleavage of trityl protecting groups may occur. See also Appendix 6. For further discussion of this and other photo-removable protecting groups, see: Synthesis, 1 (1980); Org. Photochem., 9, 225 (1987).