97966-31-9

Basic information

• Product Name: Methyl 3-ethoxy-4-Methoxybenzoate
• Synonyms: Methyl 3-ethoxy-4-Methoxybenzoate;methyl 3-ethoxy-4-methoxybenzoate(WX192030)
• CAS NO: 97966-31-9
• Molecular Formula: C₁₁H₁₄O₄
• Molecular Weight: 210.22646
• Mol File: 97966-31-9.mol
• Article Data: 10

Chemical Properties

• Melting Point: 81-83 °C
• Boiling Point: 300.1±22.0 °C(Predicted)
• Appearance: /
• Density: 1.095±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Methyl 3-ethoxy-4-Methoxybenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl 3-ethoxy-4-Methoxybenzoate(97966-31-9)
• EPA Substance Registry System: Methyl 3-ethoxy-4-Methoxybenzoate(97966-31-9)

Safety Data

• Hazardous Substances Data: 97966-31-9(Hazardous Substances Data)

Upstream product

• 617-05-0 ethyl vanillate 
• 6482-24-2 2-Bromoethyl methyl ether 
• 121-34-6 3-methoxy-4-hydroxybenzoic acid 
• 74-96-4 ethyl bromide 
• 6702-50-7 3-hydroxy-4-methoxybenzoate 
• 100-39-0 benzyl bromide 
• 645-08-9 Isovanillic acid 
• 75-03-6 ethyl iodide 
• 2651-55-0 3-ethoxy-4-methoxybenzoic acid 

Downstream Products

• 2651-55-0 3-ethoxy-4-methoxybenzoic acid 
• 247568-34-9 2-fluoro-5-nitro-N-(1,3-benzodioxol-5-ylmethyl)benzamide 
• 247566-96-7 2-(tert-Butylamino)-5-nitro-N-(1,3-benzodioxol-5-ylmethyl)benzamide 
• 247567-01-7 2-(tert-Butoxyamino)-5-nitro-N-(1,3-benzodioxol-5-ylmethyl)benzamide 
• 108439-67-4 3-ethoxy-4-methoxybenzylamine 
• 247569-89-7 3-ethoxy-4-methoxy-benzoic acid amide 
• 60758-86-3 3-ethoxy-4-methoxybenzenecarbonitrile 

Relevant articles and documents

Method for synthesizing 1-(3-ethyoxyl-4-methoxy)phenyl-2-methyl-sulfonyl ethylamine

The invention discloses a method for synthesizing 1-(3-ethyoxyl-4-methoxy)phenyl-2-methyl-sulfonyl ethylamine and belongs to the technical field of organic synthesis processes. The method comprises the following steps: taking 3-hydroxy-4-methoxybenzoic acid as a raw material, carrying out an esterification reaction to obtain 3-hydroxy-4-methoxybenzoate, reacting with bromoethane to obtain 3-ethyoxyl-4-methoxybenzoate, then reacting with dimethyl sulfone to obtain 1-(3-ethyoxyl-4-methoxy)phenyl-2-methyl sulfonyl ethyl ketone, and finally carrying out a reductive amination reaction with ammoniumformate, thereby obtaining the 1-(3-ethyoxyl-4-methoxy)phenyl-2-methyl-sulfonyl ethylamine.

USE OF CYANOQUINOLINES FOR TREATING OR INHIBITING COLONIC POLYPS

This invention provides a method of treating or inhibiting colonic polyps which comprises providing a compound of formula (1); wherein R1, R2, R3, R4, X, Y, and n are defined hereinbefore, or a pharmaceutically acceptable salt thereof.

SUBSTITUTED 3-CYANOQUINOLINES AS PROTEIN TYROSINE KINASES INHIBITORS

This invention provides compounds of formula (1) wherein R1, G1, G2, R4, Z, X and n are defined herein, or a pharmaceutically acceptable salt thereof, which are useful as antineoplastic agents and in the treatment of polycystic kidney disease.