910032-81-4

Basic information

• Product Name: [4-(3-bromo-propoxy)-2-methyl-phenoxy]-acetic acid methyl ester
• Synonyms: [4-(3-bromo-propoxy)-2-methyl-phenoxy]-acetic acid methyl ester
• CAS NO: 910032-81-4
• Molecular Weight: 317.18
• Mol File: 910032-81-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: [4-(3-bromo-propoxy)-2-methyl-phenoxy]-acetic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: [4-(3-bromo-propoxy)-2-methyl-phenoxy]-acetic acid methyl ester(910032-81-4)
• EPA Substance Registry System: [4-(3-bromo-propoxy)-2-methyl-phenoxy]-acetic acid methyl ester(910032-81-4)

Safety Data

• Hazardous Substances Data: 910032-81-4(Hazardous Substances Data)

Upstream product

• 910032-99-4 4-(3-bromo-propoxy)-2-methyl-phenol 
• 96-32-2 bromoacetic acid methyl ester 
• 109-64-8 1,3-dibromo-propane 
• 317319-10-1 methyl (4-hydroxy-2-methylphenoxy)acetate 
• 100927-02-4 4-(benzyloxy)-3-methylphenol 
• 56443-69-7 1-(4-(benzyloxy)-3-methylphenyl)ethanone 
• 876-02-8 4-hydroxy-3-methylphenyl methyl ketone 
• 910032-98-3 1-Benzyloxy-4-(3-bromo-propoxy)-2-methyl-benzene 
• 944313-42-2 acetic acid 4-benzyloxy-3-methyl-phenyl ester 

Downstream Products

• 910033-02-2 {2-methyl-4-[3-(4-propyl-6-trifluoromethyl-pyridin-3-yloxy)-propoxy]-phenoxy}-acetic acid methyl ester 
• 910032-87-0 {2-methyl-4-[3-(2-propyl-4-trifluoromethyl-phenoxy)-propoxy]-phenoxy}-acetic acid methyl ester 

Relevant articles and documents

Novel bisaryl substituted thiazoles and oxazoles as highly potent and selective peroxisome proliferator-activated receptor δ agonists

The discovery, synthesis, and optimization of compound 1 from a high-throughput screening hit to highly potent and selective peroxisome proliferator-activated receptor δ (PPARδ) agonists are reported. The synthesis and structure-activity relationship in this series are described in detail. On the basis of a general schematic PPAR pharmacophore model, scaffold 1 was divided into headgroup, linker, and tailgroup and successively optimized for PPAR activation using in vitro PPAR transactivation assays. A (2-methylphenoxy)acetic acid headgroup, a flexible linker, and a five-membered heteroaromatic center ring with two hydrophobic aryl substituents were required for efficient and selective PPARδ activation. The fine-tuning of these aryl substituents led to an array of highly potent and selective compounds such as compound 38c, displaying an excellent pharmacokinetic profile in mouse. In an in vivo acute dosing model, selected members of this array were shown to induce the expression of pyruvate dehydrogenase kinase-4 (PDK4) and uncoupling protein-3 (UCP3), genes that are known to be involved in energy homeostasis and regulated by PPARδ in skeletal muscle.