29056-05-1

Basic information

• Product Name: 4-(1-METHYLETHOXY)-BENZENEACETIC ACID METHYL ESTER
• Synonyms: 4-(1-METHYLETHOXY)-BENZENEACETIC ACID METHYL ESTER;BENZENEACETIC ACID, 4-(1-METHYLETHOXY)-, METHYL ESTER
• CAS NO: 29056-05-1
• Molecular Formula: C₁₂H₁₆O₃
• Molecular Weight: 208.26
• Mol File: 29056-05-1.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 283.2±15.0 °C(Predicted)
• Appearance: /
• Density: 1.043±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 4-(1-METHYLETHOXY)-BENZENEACETIC ACID METHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(1-METHYLETHOXY)-BENZENEACETIC ACID METHYL ESTER(29056-05-1)
• EPA Substance Registry System: 4-(1-METHYLETHOXY)-BENZENEACETIC ACID METHYL ESTER(29056-05-1)

Safety Data

• Hazardous Substances Data: 29056-05-1(Hazardous Substances Data)

Upstream product

• 14199-15-6 Methyl 4-hydroxyphenylacetate 
• 75-26-3 isopropyl bromide 
• 75-30-9 2-iodo-propane 
• 156-38-7 4-hydroxyphenylacetate 
• 67-56-1 methanol 
• 55784-07-1 4-hydroxyphenylacetic acid isopropyl ether 

Downstream Products

• 158816-13-8 (R,S)-2-<4-(isopropoxy)phenyl>propanoic acid methyl ester 
• 3585-60-2 2-(4-Isopropoxy-phenyl)-propionic acid 
• 110319-81-8 N-Hydroxy-2-(4-isopropoxy-phenyl)-N-methyl-propionamide 
• 55784-07-1 4-hydroxyphenylacetic acid isopropyl ether 
• 1428054-81-2 C₄₅H₈₇NO₁₅Si₈ 
• 1428054-75-4 methyl 2-(3-bromo-4-isopropoxyphenyl)acetate 
• 1428054-77-6 methyl 2-(4-isopropoxy-3-vinylphenyl)acetate 
• 1428054-78-7 2-(4-isopropoxy-3-vinylphenyl)ethanol 
• 1409950-43-1 1,7-difluoro-3-(4-isopropoxyphenyl)-6-methoxyisoquinoline 
• 1409950-44-2 (E)-3-(4-fluoro-3-methoxyphenyl)-2-(4-isopropoxyphenyl)acrylic acid 
• 1409950-45-3 (E)-3-(4-fluoro-3-methoxyphenyl)-2-(4-isopropoxyphenyl)acryloyl azide 
• 1409950-46-4 7-fluoro-3-(4-isopropoxyphenyl)-6-methoxyisoquinolin-1-ol 
• 1409950-47-5 1-chloro-7-fluoro-3-(4-isopropoxyphenyl)-6-methoxyisoquinoline 

Relevant articles and documents

Palladium-catalyzed intermolecular C-H silylation initiated by aminopalladation

A Pd(ii)-catalyzed intermolecular C-H silylation reaction initiated by aminopalladation has been developed. The C-H bonds were activated by an alkyl Pd(ii) species generated through aminopalladation and then disilylated with hexamethyldisilane to form disilylated indolines as the final products. The reaction provides a new method for the introduction of silyl groups into complex organic molecules.

Hepatitis C virus inhibitors

Hepatitis C virus inhibitors having the general formula (I) are disclosed. Compositions comprising the compounds and methods for using the compounds to inhibit HCV are also disclosed.

Hepatitis C Virus Inhibitors

Hepatitis C virus inhibitors having the general formula (I) are disclosed. Compositions comprising the compounds and methods for using the compounds to inhibit HCV are also disclosed.