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(E)-4-((3-(pyridin-3-yl)acrylaMido)Methyl)benzoic acid

Base Information
  • Chemical Name:(E)-4-((3-(pyridin-3-yl)acrylaMido)Methyl)benzoic acid
  • CAS No.:219964-34-8
  • Molecular Formula:C16H14N2O3
  • Molecular Weight:282.299
  • Hs Code.:
  • Mol file:219964-34-8.mol
(E)-4-((3-(pyridin-3-yl)acrylaMido)Methyl)benzoic acid

Synonyms:Benzoic acid, 4-[[[1-oxo-3-(3-pyridinyl)-2-propenyl]amino]methyl]- (9CI);Benzoic acid, 4-[[[1-oxo-3-(3-pyridinyl)-2-propen-1-yl]amino]methyl]-;

Suppliers and Price of (E)-4-((3-(pyridin-3-yl)acrylaMido)Methyl)benzoic acid
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
  • TRC
  • E-4-((3-(Pyridin-3-yl)acrylamido)methyl)benzoicAcid
  • 500mg
  • $ 580.00
  • TRC
  • E-4-((3-(Pyridin-3-yl)acrylamido)methyl)benzoicAcid
  • 100mg
  • $ 160.00
Total 4 raw suppliers
Chemical Property of (E)-4-((3-(pyridin-3-yl)acrylaMido)Methyl)benzoic acid
Chemical Property:
  • PSA:79.29000 
  • LogP:2.50030 
Purity/Quality:

Purity more than 98% *data from raw suppliers

E-4-((3-(Pyridin-3-yl)acrylamido)methyl)benzoicAcid *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses E-4-((3-(Pyridin-3-yl)acrylamido)methyl)benzoic Acid acts as a reagent for the synthesis of chidamide, a new histone deacetylase (HDAC) inhibitor.
Technology Process of (E)-4-((3-(pyridin-3-yl)acrylaMido)Methyl)benzoic acid

There total 4 articles about (E)-4-((3-(pyridin-3-yl)acrylaMido)Methyl)benzoic 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:
trans-3-(3-pyridyl)acrylic acid; With 1,1'-carbonyldiimidazole; In tetrahydrofuran; at 0 - 20 ℃; for 3h;
p-aminomethylbenzoic acid; With sodium hydroxide; In tetrahydrofuran; water; at 20 ℃; for 8h;
Guidance literature:
p-aminomethylbenzoic acid; With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine; In acetonitrile; at 20 ℃; for 0.5h;
p-aminomethylbenzoic acid; With sodium hydroxide; In acetonitrile; at 60 ℃;
With hydrogenchloride; In water; acetonitrile; pH=7;
Guidance literature:
3-(pyridin-3-yl)acrylic acid; With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine; In acetonitrile; at 20 ℃; for 0.5h;
p-aminomethylbenzoic acid; With sodium hydroxide; In water; acetonitrile; at 60 ℃; for 1h;
With hydrogenchloride; In water; acetonitrile; pH=7;
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