Phenoxyacetic acid derivatives
Sigma Aldrich 4-(Aminomethyl)hepta-1,6-dien-4-ol hydrochloride
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
Sigma Aldrich 5-Formyluracil
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
Sigma Aldrich 1H-Imidazol-1-ylacetic acid
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
Medchemexpress LLC AP1867-2-carboxymeth 100mg | 2230613-03-1 | 100 MG
AP1867-2-(carboxymethoxy) is a PROTAC FKBP12-binding moiety based on the synthetic FKBP12F36V-directed ligand AP1867, intended for research use in assembling dTAG molecules that engage FKBP12F36V and CRBN in vitro.
- High purity for reliable assay results.
- Molecular weight 693.78 g/mol.
- Chemical formula C38H47NO11.
- Designed to link to CRBN ligands to form dTAG molecules.
- Available in multiple pack sizes for assay development.
Chem-Impex International, Inc. Phenoxyacetic anhydride | 14316-61-1 | MFCD00059681 | 5G
Phenoxyacetic anhydride, 14316-61-1, MFCD00059681, 5G
eMolecules 2-(3,5-Dimethoxyphenoxy)-1-phenylethanol | 1183425-15-1 | | 250mg
Ambeed | 2-(3,5-Dimethoxyphenoxy)-1-phenylethanol | 250mg | 600829855 | A1351485 | | 1183425-15-1 | | 274.316 | C16H18O4
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Sigma Aldrich Fine Chemicals Biosciences SR-58611A >=98% (HPLC) | 121524-09-2 | MFCD00886563 | 5MG
SR-58611A >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 440.36 | 121524-09-2 | MFCD00886563 | 5MG
Chem-Impex International, Inc. 4-(Hydroxymethyl)phenoxyacetic acid | 68858-21-9 | MFCD00057827 | 5G
4-(Hydroxymethyl)phenoxyacetic acid, 68858-21-9, MFCD00057827, 5G
Medchemexpress LLC HY-B0637 100mg , Bezafibrate BM15075 CAS:41859-67-0 Purity:98%
Medchemexpress, HY-B0637 100mg Bezafibrate BM15075 CAS:41859-67-0 Formula:C19H20ClNO4 EC50: 90 μM (Murine PPARα), 55 μM (Murine PPARγ), 110 μM (Murine PPARδ), 50 μM (Human PPARα), 60 μM (Human PPARγ), 20 μM (Human PPARδ) Purity:98% Bezafibrate is an agonist of PPAR , with EC 50 s of 50 μM, 60 μM, 20 μM for human PPARα , PPARγ and PPARδ , and 90 μM, 55 μM, 110 μM for murine PPARα , PPARγ and PPARδ , respectively; Bezafibrate is used as an hypolipidemic agent. Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Medchemexpress LLC HY-114434 10mg Medchemexpress, AP1867 CAS:195514-23-9 Purity:>98%
Medchemexpress, HY-114434 10mg AP1867 CAS:195514-23-9 AP1867 is a synthetic FKBP12F36V-directed ligand. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Medchemexpress LLC 2-naphthoxyacetic acid | 120-23-0 | MFCD00004066 | 99.9% | 202.21 g/mol | C12H10O3 | 50 G
2-Naphthoxyacetic acid is a small aromatic carboxylic acid used as a research-grade endogenous metabolite standard and reagent. It is supplied as a solid and as DMSO solutions for biochemical, analytical, and metabolic studies.
- High purity (99.89%) suitable for analytical applications.
- Molecular weight 202.21 g/mol and formula C12H10O3.
- Available in multiple pack sizes to support bench-scale and bulk needs.
- White to off-white solid with good solubility in DMSO.
- Commonly used as a reference standard and in metabolite profiling workflows.
Research Products International Corp B-Naphthoxyacetic Acid, 100 Grams
Molecular Formula: C12H10O3
MW 202.2