154534-98-2

Basic information

• Product Name: ethyl 2-bromo-2-(2-bromo-4,5-dimethoxyphenyl)acetate
• Synonyms: ethyl 2-bromo-2-(2-bromo-4,5-dimethoxyphenyl)acetate
• CAS NO: 154534-98-2
• Molecular Weight: 382.049
• Mol File: 154534-98-2.mol

Chemical Properties

• CAS DataBase Reference: ethyl 2-bromo-2-(2-bromo-4,5-dimethoxyphenyl)acetate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2-bromo-2-(2-bromo-4,5-dimethoxyphenyl)acetate(154534-98-2)
• EPA Substance Registry System: ethyl 2-bromo-2-(2-bromo-4,5-dimethoxyphenyl)acetate(154534-98-2)

Safety Data

• Hazardous Substances Data: 154534-98-2(Hazardous Substances Data)

Upstream product

• 18066-68-7 ethyl 3,4-dimethoxyphenylacetate 
• 91881-19-5 ethyl (2-bromo-4,5-dimethoxyphenyl)acetate 

Downstream Products

• 154535-03-2 ethyl -2-(2-bromo-4,5-dimethoxyphenyl)acetate 
• 154535-04-3 -2-(2-bromo-4,5-dimethoxyphenyl)acetic acid 
• 154535-01-0 ethyl 2--2-(2-bromo-4,5-dimethoxyphenyl)acetate 
• 154535-06-5 2-(3,4-dimethoxyphenyl)-2,3,4,5-tetrahydro-7,8-dimethoxy-3-benzazepin-1-one 
• 154535-00-9 ethyl 2-<2-(3,4-dimethoxyphenyl)ethylamino>-2-(2-bromo-4,5-dimethoxyphenyl)acetate 

Relevant articles and documents

Synthesis of saulatine

A study directed toward the synthesis of saulatine (5,8,9,14a-tetrahydro- 3,4,11,12-tetramethoxy-isoquino[1,2-b]benzazepine-6,14-dione) is described. The successful synthetic route consists of three steps starting with 3,4- dimethoxyphenethylamine and 2-bromo-(3,4-dimethoxy-2- ethoxycarbomethylphenyl)-acetate. It was found that the methoxy moieties present on the aromatic rings prohibit the use of the intramolecular Friedel- Crafts reaction with a Lewis acid catalyst for ring construction because of their demethylation tendency under the reaction conditions.