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2-(3-bromo-2-nitrophenyl)acetic acid

Base Information Edit
  • Chemical Name:2-(3-bromo-2-nitrophenyl)acetic acid
  • CAS No.:400629-31-4
  • Molecular Formula:C8H6BrNO4
  • Molecular Weight:260.044
  • Hs Code.:
  • Mol file:400629-31-4.mol
2-(3-bromo-2-nitrophenyl)acetic acid

Synonyms:2-(3-bromo-2-nitrophenyl)acetic acid

Suppliers and Price of 2-(3-bromo-2-nitrophenyl)acetic acid
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Total 2 raw suppliers
Chemical Property of 2-(3-bromo-2-nitrophenyl)acetic acid Edit
Chemical Property:
Purity/Quality:

98% *data from raw suppliers

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Technology Process of 2-(3-bromo-2-nitrophenyl)acetic acid

There total 4 articles about 2-(3-bromo-2-nitrophenyl)acetic acid 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:
Guidance literature:
With hydrogenchloride; In water; acetone; Solvent; Reflux;
Guidance literature:
C8H8BrNO2; With sodium hydrogencarbonate; sodium hydroxide; at 0 ℃; for 0.166667h; Inert atmosphere; Darkness;
With Oxone; ethylenediaminetetraacetic acid; In water; acetone; for 4h; Cooling with ice; Inert atmosphere; Darkness;
DOI:10.1039/c5ra04984a
Guidance literature:
Multi-step reaction with 2 steps
1.1: hydrazine hydrate / diethylene glycol / 1 h / 80 °C / Inert atmosphere
1.2: 2 h / 120 °C / Inert atmosphere
1.3: Inert atmosphere
2.1: sodium hydroxide; sodium hydrogencarbonate / 0.17 h / 0 °C / Inert atmosphere; Darkness
2.2: 4 h / Cooling with ice; Inert atmosphere; Darkness
With sodium hydrogencarbonate; hydrazine hydrate; sodium hydroxide; In diethylene glycol; 1.1: |Wolff-Kishner Reduction;
DOI:10.1039/c5ra04984a
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