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1-aMino-4-broMo-2-naphthoic acid

Base Information Edit
  • Chemical Name:1-aMino-4-broMo-2-naphthoic acid
  • CAS No.:1227924-42-6
  • Molecular Formula:C11H8BrNO2
  • Molecular Weight:266.094
  • Hs Code.:
  • Mol file:1227924-42-6.mol
1-aMino-4-broMo-2-naphthoic acid

Synonyms:1-aMino-4-broMo-2-naphthoic acid

Suppliers and Price of 1-aMino-4-broMo-2-naphthoic acid
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • 1-Amino-4-bromonaphthalene-2-carboxylicAcid
  • 5mg
  • $ 45.00
  • Matrix Scientific
  • 1-Amino-4-bromonaphthalene-2-carboxylic acid 95%
  • 5g
  • $ 1980.00
  • Alichem
  • 1-Amino-4-bromo-2-naphthoicacid
  • 1g
  • $ 1140.72
  • Alichem
  • 1-Amino-4-bromo-2-naphthoicacid
  • 250mg
  • $ 470.66
  • A1 Biochem Labs
  • 1-Amino-4-bromonaphthalene-2-carboxylicacid 95%
  • 5 g
  • $ 1200.00
Total 1 raw suppliers
Chemical Property of 1-aMino-4-broMo-2-naphthoic acid Edit
Chemical Property:
  • PSA:63.32000 
  • LogP:3.46390 
Purity/Quality:

95+% *data from raw suppliers

1-Amino-4-bromonaphthalene-2-carboxylicAcid *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of 1-aMino-4-broMo-2-naphthoic acid

There total 8 articles about 1-aMino-4-broMo-2-naphthoic 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 N-Bromosuccinimide; In tetrahydrofuran; water; N,N-dimethyl-formamide; at 0 - 15 ℃; for 1h;
Guidance literature:
With alkali metal hydroxide; In tetrahydrofuran; water; at 50 - 90 ℃; for 22h; Inert atmosphere;
DOI:10.1021/acsmedchemlett.8b00095
Guidance literature:
Multi-step reaction with 6 steps
1.1: toluene / 39 h / 120 °C
2.1: potassium carbonate; potassium permanganate / water; tert-butyl alcohol / 17.5 h / 20 °C
3.1: hydrogenchloride / 42 h / 0 - 90 °C
4.1: hydrogen / palladium on activated charcoal / tetrahydrofuran; methanol / 14 h / 760.05 Torr
5.1: bromine / 1,4-dioxane; tetrachloromethane / 2 h / 0 °C
6.1: sodium hydroxide / water; tetrahydrofuran / 22 h / 50 - 90 °C
6.2: 2 h
With hydrogenchloride; potassium permanganate; hydrogen; bromine; potassium carbonate; sodium hydroxide; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; methanol; tetrachloromethane; water; toluene; tert-butyl alcohol;
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