Search Thermo Fisher Scientific
Phenol esters
Organic compounds that consist of a phenyl ring with an ester functional group substitution; ester functional groups contain an oxygen atom bonded to a carbonyl group subsequently bonded to a methyl group.
Products (19)
Learn More (13)
Documents & Support
(25)19 Products
Filter
This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to...
This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to...
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...
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...
m-Tolyl acetate as a pharmaceutical intermediate and antiseptic. 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.
Phenyl bromoacetate may be employed as alkylation reagent in the preparation of 2-(phenoxycarbonyl)methyl triazoles. It may be used in the synthesis of the A-ring of cylindrospermopsin and in the synthesis of...
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...
Phenyl acrylate reacts with benzaldehyde to produce 2-(hydroxy-phenyl-methyl)-acrylic acid phenyl ester. 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.
4-Nitrophenyl acetate is used with iodoacetic acid for reductive cleavage of methionine-containing peptides. It is also used as a substrate that has been used in assays for esterase and lipase activity.
This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to...
This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to...
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...
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...
The activities of free and immobilized PPL were determined by spectrophotometric assay using 4-nitrophenyl palmitate (pNPP) as substrate. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio.
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...
Learn More (13)
View all
In the early 1900s, K. Fries and colleagues reacted phenolic esters of acetic and chloroacetic acid with aluminum chloride, isolating a mixture of ortho- and para-acetyl and chloroacetyl phenols. Fries realized that this rearrangement of phenolic esters was general, and for this the transformation...
In 1912, German chemist Rainer Ludwig Claisen published the rearrangement of allyl phenyl ethers to their corresponding C-allyl phenols, as well as the conversion of the O-allylated acetoacetic ester to its C-allylated isomer upon treatment with ammonium chloride, followed by distillation.
Documents & Support (25)
View all
Introduction to Amine Modification—Section 1.1
Reagents for Modifying Alcohols—Section 3.2