1-bromo-4-hydroxy-7-phenoxyisoquinoline-3-carboxylic acid methyl ester

Base Information

Chemical Name:1-bromo-4-hydroxy-7-phenoxyisoquinoline-3-carboxylic acid methyl ester
CAS No.:1455091-21-0
Molecular Formula:C₁₇H₁₂BrNO₄
Molecular Weight:374.191
Hs Code.:

Synonyms:1-bromo-4-hydroxy-7-phenoxyisoquinoline-3-carboxylic acid methyl ester

Suppliers and Price of 1-bromo-4-hydroxy-7-phenoxyisoquinoline-3-carboxylic acid methyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Total 10 raw suppliers

Chemical Property of 1-bromo-4-hydroxy-7-phenoxyisoquinoline-3-carboxylic acid methyl ester

Chemical Property:

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

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Hazard Codes:

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Technology Process of 1-bromo-4-hydroxy-7-phenoxyisoquinoline-3-carboxylic acid methyl ester

There total 6 articles about 1-bromo-4-hydroxy-7-phenoxyisoquinoline-3-carboxylic acid methyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 93.9%

: 1455091-10-7
4-hydroxy-7-phenoxyisoquinoline-3-carboxylic acid methyl ester

: 1455091-21-0
1-bromo-4-hydroxy-7-phenoxyisoquinoline-3-carboxylic acid methyl ester

Guidance literature:: With N-Bromosuccinimide; In dichloromethane; at 0 - 20 ℃;

Reference yield:

: 1455091-04-9
2-(chloromethyl)-4-phenoxybenzoic acid methyl ester

: 1455091-21-0
1-bromo-4-hydroxy-7-phenoxyisoquinoline-3-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate; sodium iodide / N,N-dimethyl-formamide / 50 °C

2: sodium methylate / dimethyl sulfoxide; methanol / 0.5 h / 20 °C

3: N-Bromosuccinimide; dibenzoyl peroxide / tetrachloromethane / 1 h / Reflux

With N-Bromosuccinimide; sodium methylate; potassium carbonate; sodium iodide; dibenzoyl peroxide; In methanol; tetrachloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide;

Reference yield:

: 1455091-06-1
2-{[(methoxycarbonylmethyl)(toluene-4-sulfonyl)amino]methyl}-4-phenoxybenzoic acid methyl ester

: 1455091-21-0
1-bromo-4-hydroxy-7-phenoxyisoquinoline-3-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: sodium methylate / dimethyl sulfoxide; methanol / 0.5 h / 20 °C

2: N-Bromosuccinimide; dibenzoyl peroxide / tetrachloromethane / 1 h / Reflux

With N-Bromosuccinimide; sodium methylate; dibenzoyl peroxide; In methanol; tetrachloromethane; dimethyl sulfoxide;