Methyl 7-bromo-1H-indazole-5-carboxylate

Base Information

• Chemical Name: Methyl 7-bromo-1H-indazole-5-carboxylate
• CAS No.: 1427460-96-5
• Molecular Formula: C9H7BrN2O2
• Molecular Weight: 255.071
• Hs Code.: 2933998090
• Mol file: 1427460-96-5.mol

Synonyms:Methyl 7-bromo-1H-indazole-5-carboxylate;7-Bromo-1H-indazole-5-carboxylic acid methyl ester

Chemical Property of Methyl 7-bromo-1H-indazole-5-carboxylate

Chemical Property:

• PSA: 54.98000
• LogP: 2.11200
• Storage Temp.: Inert atmosphere,Room Temperature

Purity/Quality:

99%, ^*data from raw suppliers

Methyl7-Bromo-1h-Indazole-5-Carboxylate ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of Methyl 7-bromo-1H-indazole-5-carboxylate

There total 2 articles about Methyl 7-bromo-1H-indazole-5-carboxylate 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: 25.0%

methyl 4-amino-3-bromo-5-methylbenzoate (900019-52-5) → methyl 7-bromo-1H-indazole-5-carboxylate (1427460-96-5)

Guidance literature:

With acetic acid; sodium nitrite; In water; at 20 ℃; for 5h;

Reference yield:

methyl 4-amino-3-methylbenzoate (18595-14-7) → methyl 7-bromo-1H-indazole-5-carboxylate (1427460-96-5)

Guidance literature:

Multi-step reaction with 2 steps

1: N-Bromosuccinimide / dichloromethane / 3 h / 20 °C

2: sodium nitrite; acetic acid / water / 5 h / 20 °C

With N-Bromosuccinimide; acetic acid; sodium nitrite; In dichloromethane; water;

Reference yield: 65.0%

3,4-difluoronitrobenzene (369-34-6) + methyl 7-bromo-1H-indazole-5-carboxylate (1427460-96-5) → methyl 7-bromo-2-(2-fluoro-4-nitrophenyl)-2H-indazole-5-carboxylate

Guidance literature:

With potassium carbonate; In acetonitrile; at 80 ℃; for 18h;

upstream raw materials:

methyl 4-amino-3-methylbenzoate

methyl 4-amino-3-bromo-5-methylbenzoate

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