76322-06-0

Basic information

• Product Name: Acetic acid, (2-formyl-5-methoxyphenoxy)-, ethyl ester
• CAS NO: 76322-06-0
• Molecular Formula: C12H14O5
• Molecular Weight: 238.24
• Mol File: 76322-06-0.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Acetic acid, (2-formyl-5-methoxyphenoxy)-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Acetic acid, (2-formyl-5-methoxyphenoxy)-, ethyl ester(76322-06-0)
• EPA Substance Registry System: Acetic acid, (2-formyl-5-methoxyphenoxy)-, ethyl ester(76322-06-0)

Safety Data

• Hazardous Substances Data: 76322-06-0(Hazardous Substances Data)

Upstream product

• 673-22-3 2-Hydroxy-4-methoxybenzaldehyde 
• 105-36-2 ethyl bromoacetate 
• 95-01-2 2,4-Dihydroxybenzaldehyde 

Downstream Products

• 158073-00-8 2-carboethoxymethoxy-4-methoxybenzyl alcohol 
• 13196-11-7 6-hydroxybenzofuran 
• 50551-61-6 6-methoxybenzofuran-2-carboxylic acid 
• 76322-19-5 ethyl(2-ethoxycarbonylmethoxy-4-methoxyphenyl)acetate 
• 115124-43-1 (2-carboxymethoxy-4-methoxy-phenyl)-acetic acid 
• 76322-24-2 7-methoxychroman-3-one 
• 76322-11-7 (2-ethoxycarbonylmethoxy-4-methoxyphenyl)hydroxyacetonitrile 
• 856357-86-3 2-(2-formyl-5-methoxyphenoxy)acetic acid 
• 50551-57-0 ethyl 6-methoxybenzo[b]furan-2-carboxylate 

Relevant articles and documents

An improved and scale-up synthesis of 6-hydroxybenzofuran

An optimized process for the preparation of 6-hydroxybenzofuran is described. This process consists of three steps: the reaction of 2-hydroxy-4-methoxybenzaldehyde with chloroacetic acid, the formation of the 6-methoxybenzofuran in acetic anhydride, and t

Rhodium-Catalyzed Intermolecular Cyclopropanation of Benzofurans, Indoles, and Alkenes via Cyclopropene Ring Opening

The generation of metal carbenoids via ring opening of cyclopropenes by transition metals offers a simple entry into highly reactive intermediates. Herein, we describe a diastereoselective intermolecular rhodium-catalyzed cyclopropanation of heterocycles and alkenes using cyclopropenes as carbene precursors with a low loading of a commercially available rhodium catalyst. The reported method is scalable and could be performed with catalyst loadings as low as 0.2 mol %, with no impact to the reaction yield or selectivity.

S1P RECEPTORS MODULATORS

The invention relates to novel compounds that have S1P receptor modulating activity and, preferably, apoptotic activity and/or anti proliferative activity against cancer cells and other cell types. Further, the invention relates to a pharmaceutical comprising at least one compound of the invention for the treatment of diseases and/or conditions caused by or associated with inappropriate S1P receptor modulating activity or expression, for example, cancer. A further aspect of the invention relates to the use of a pharmaceutical comprising at least one compound of the invention for the manufacture of a medicament for the treatment of diseases and/or conditions caused by or associated with inappropriate S1P receptor modulating activity or expression such as cancer.