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N-[(4-methoxyphenyl)methyl]pyrimidin-2-amine

Base Information
  • Chemical Name:N-[(4-methoxyphenyl)methyl]pyrimidin-2-amine
  • CAS No.:6957-21-7
  • Molecular Formula:C12H13 N3 O
  • Molecular Weight:215.255
  • Hs Code.:2933599090
  • Mol file:6957-21-7.mol
N-[(4-methoxyphenyl)methyl]pyrimidin-2-amine

Synonyms:Pyrimidine,2-[(p-methoxybenzyl)amino]- (7CI,8CI); NSC 66170

Suppliers and Price of N-[(4-methoxyphenyl)methyl]pyrimidin-2-amine
Supply Marketing:
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
  • Sigma-Aldrich
  • 2-(4-METHOXYBENZYLAMINO)PYRIMIDINE AldrichCPR
  • 1g
  • $ 144.00
  • Crysdot
  • N-(4-Methoxybenzyl)pyrimidin-2-amine 95+%
  • 5g
  • $ 671.00
  • Chemenu
  • N-(4-methoxybenzyl)pyrimidin-2-amine 95%
  • 5g
  • $ 634.00
Total 12 raw suppliers
Chemical Property of N-[(4-methoxyphenyl)methyl]pyrimidin-2-amine
Chemical Property:
  • Vapor Pressure:1.16E-06mmHg at 25°C 
  • Melting Point:97-99 °C 
  • Boiling Point:401.7°C at 760 mmHg 
  • PKA:3.55±0.10(Predicted) 
  • Flash Point:196.7°C 
  • PSA:47.04000 
  • Density:1.195g/cm3 
  • LogP:2.17030 
Purity/Quality:

99.90% *data from raw suppliers

2-(4-METHOXYBENZYLAMINO)PYRIMIDINE AldrichCPR *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses N-(4-Methoxybenzyl)-2-pyrimidinamine acts as a reagent in the preparation of 2-(Benzylidineamino)pyrimidines as an antihistaminic agents.
Technology Process of N-[(4-methoxyphenyl)methyl]pyrimidin-2-amine

There total 14 articles about N-[(4-methoxyphenyl)methyl]pyrimidin-2-amine 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 C31H25ClN3NiOP; potassium hydroxide; In toluene; at 120 ℃; for 24h; Schlenk technique; Inert atmosphere; Green chemistry;
DOI:10.1021/acs.joc.0c00530
Guidance literature:
With potassium fluoride; In water; at 100 ℃; for 17h; Green chemistry;
DOI:10.1002/cssc.201300239
Guidance literature:
With triethylamine; In ethanol; at 120 ℃; for 0.0833333h; microwave irradiation;
DOI:10.1021/jo8008758
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