100059-20-9

Basic information

• Product Name: Benzeneacetic acid, 4-(methoxymethoxy)-, methyl ester
• CAS NO: 100059-20-9
• Molecular Formula: C11H14O4
• Molecular Weight: 210.23
• Mol File: 100059-20-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzeneacetic acid, 4-(methoxymethoxy)-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzeneacetic acid, 4-(methoxymethoxy)-, methyl ester(100059-20-9)
• EPA Substance Registry System: Benzeneacetic acid, 4-(methoxymethoxy)-, methyl ester(100059-20-9)

Safety Data

• Hazardous Substances Data: 100059-20-9(Hazardous Substances Data)

Upstream product

• 14199-15-6 Methyl 4-hydroxyphenylacetate 
• 107-30-2 chloromethyl methyl ether 
• 13057-17-5 bromethyl methyl ether 

Downstream Products

• 126716-61-8 2-(4-(methoxymethoxy)phenyl)ethanol 
• 14199-15-6 Methyl 4-hydroxyphenylacetate 
• 102946-37-2 (4-methoxymethoxy-phenyl)-acetic acid-(4-benzyloxy-3-methoxy-phenethylamide) 

Relevant articles and documents

SUPPRESSION AND REGENERATION PROMOTING EFFECT OF LOW MOLECULAR WEIGHT COMPOUND ON CANCER AND FIBROSIS

To obtain a novel therapeutic drug for a malignant tumor or fibrosis. Used is a compound represented by formula (1), a salt thereof, or a solvate thereof. Also used is a therapeutic drug for a malignant tumor or a therapeutic drug for fibrosis, comprising

Serotonin derivatives as a new class of non-ATP-competitive receptor tyrosine kinase inhibitors

The discovery of new templates and their subsequent elaboration to clinically useful receptor tyrosine kinase (RTK) inhibitors continues to be an important issue. RTKs are a class of enzymes responsible for the activation of different cellular signal transduction cascades. The majority of the known small molecules RTK inhibitors are ATP-competitive and they are multiple targeted inhibitors. We describe here serotonin derivatives as a new class of multiple targeted RTK inhibitors. In contrast to most other RTK inhibitors they act via a non-ATP-competitive (allosteric) mechanism. Furthermore, they are able to inhibit the proliferation of HUVE cells, fibroblasts and two cancer cell lines.