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2-ANILINOPYRIMIDINE-5-CARBOXYLIC ACID

Base Information Edit
  • Chemical Name:2-ANILINOPYRIMIDINE-5-CARBOXYLIC ACID
  • CAS No.:450368-25-9
  • Molecular Formula:C11H9 N3 O2
  • Molecular Weight:215.21
  • Hs Code.:2933599090
  • Mol file:450368-25-9.mol
2-ANILINOPYRIMIDINE-5-CARBOXYLIC ACID

Synonyms:2-(Phenylamino)pyrimidine-5-carboxylicacid

Suppliers and Price of 2-ANILINOPYRIMIDINE-5-CARBOXYLIC 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
  • 2-Anilinopyrimidine-5-carboxylic acid
  • 100mg
  • $ 75.00
  • Sigma-Aldrich
  • 2-Anilinopyrimidine-5-carboxylic acid Aldrich
  • 1g
  • $ 140.00
  • ChemBridge Corporation
  • 2-Anilinopyrimidine-5-carboxylic acid 95%
  • 1 g
  • $ 70.00
  • American Custom Chemicals Corporation
  • 2-ANILINOPYRIMIDINE-5-CARBOXYLIC ACID 95.00%
  • 5MG
  • $ 504.45
  • AK Scientific
  • 2-Anilinopyrimidine-5-carboxylic acid
  • 1g
  • $ 224.00
Total 8 raw suppliers
Chemical Property of 2-ANILINOPYRIMIDINE-5-CARBOXYLIC ACID Edit
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Refractive Index:1.686 
  • Boiling Point:469.622ºC at 760 mmHg 
  • Flash Point:237.819ºC 
  • PSA:75.11000 
  • Density:1.393g/cm3 
  • LogP:1.99140 
Purity/Quality:

98% *data from raw suppliers

2-Anilinopyrimidine-5-carboxylic acid *data from reagent suppliers

Safty Information:
  • Pictogram(s): Xi 
  • Hazard Codes:Xi 
  • Statements: 36 
  • Safety Statements: 26 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses 2-Anilinopyrimidine-5-carboxylic Acid can be used for useful organic synthesis.
Technology Process of 2-ANILINOPYRIMIDINE-5-CARBOXYLIC ACID

There total 3 articles about 2-ANILINOPYRIMIDINE-5-CARBOXYLIC 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 water monomer; lithium hydroxide monohydrate; In tetrahydrofuran; at 20 ℃; for 12h;
DOI:10.1111/cbdd.14055
Guidance literature:
With water; lithium hydroxide; In tetrahydrofuran; methanol; at 20 ℃; for 3h;
DOI:10.1021/jm500007h
Guidance literature:
Multi-step reaction with 2 steps
1: triethylamine; palladium diacetate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene / N,N-dimethyl-formamide / 12 h / 100 °C
2: lithium hydroxide; water / tetrahydrofuran; methanol / 3 h / 20 °C
With water; palladium diacetate; triethylamine; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; lithium hydroxide; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;
DOI:10.1021/jm500007h
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