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3-(dimethylamino)-N-(3-(4-hydroxybenzamido)-4-methylphenyl)benzamide

Base Information
  • Chemical Name:3-(dimethylamino)-N-(3-(4-hydroxybenzamido)-4-methylphenyl)benzamide
  • CAS No.:208260-29-1
  • Molecular Formula:C23H23N3O3
  • Molecular Weight:389.454
  • Hs Code.:2924297099
  • DSSTox Substance ID:DTXSID70274478
  • Nikkaji Number:J1.735.950I
  • Wikidata:Q27089299
  • ChEMBL ID:CHEMBL186526
  • Mol file:208260-29-1.mol
3-(dimethylamino)-N-(3-(4-hydroxybenzamido)-4-methylphenyl)benzamide

Synonyms:N-(5-(3-dimethylaminobenzamido)-2-methylphenyl)-4-hydroxybenzamide;ZM 336372;ZM-336372;ZM336372

Suppliers and Price of 3-(dimethylamino)-N-(3-(4-hydroxybenzamido)-4-methylphenyl)benzamide
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
  • Usbiological
  • ZM 336372
  • 1mg
  • $ 323.00
  • TRC
  • ZM 336372
  • 250mg
  • $ 130.00
  • Tocris
  • ZM 336372 ≥99%(HPLC)
  • 50
  • $ 901.00
  • Tocris
  • ZM 336372 ≥99%(HPLC)
  • 10
  • $ 219.00
  • Sigma-Aldrich
  • ZM 336372 ≥98% (HPLC)
  • 25mg
  • $ 317.00
  • Sigma-Aldrich
  • ZM 336372 ≥98% (HPLC)
  • 5mg
  • $ 83.70
  • Sigma-Aldrich
  • ZM 336372 - CAS 208260-29-1 - Calbiochem
  • 1mg
  • $ 181.00
  • Labseeker
  • ZM 336372 98
  • 1g
  • $ 900.00
  • Labseeker
  • ZM 336372 98
  • 5g
  • $ 1639.00
  • DC Chemicals
  • ZM 336372 >98%
  • 1 g
  • $ 1500.00
Total 42 raw suppliers
Chemical Property of 3-(dimethylamino)-N-(3-(4-hydroxybenzamido)-4-methylphenyl)benzamide
Chemical Property:
  • Vapor Pressure:5.21E-10mmHg at 25°C 
  • Refractive Index:1.704 
  • Boiling Point:484.4 °C at 760 mmHg 
  • PKA:8.31±0.15(Predicted) 
  • Flash Point:246.8 °C 
  • PSA:81.67000 
  • Density:1.298 g/cm3 
  • LogP:4.41720 
  • Storage Temp.:-20°C 
  • Sensitive.:Light Sensitive 
  • Solubility.:DMSO: >5mg/mL (warmed) 
  • XLogP3:3.7
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:5
  • Exact Mass:389.17394160
  • Heavy Atom Count:29
  • Complexity:560
Purity/Quality:

99%, *data from raw suppliers

ZM 336372 *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=C(C=C(C=C1)NC(=O)C2=CC(=CC=C2)N(C)C)NC(=O)C3=CC=C(C=C3)O
  • Description The Ras/Raf-1 signalling pathway is a well-characterized system that links receptor tyrosine kinase (RTK) activation with changes in gene expression and cell behavior. Raf-1 is a serine/threonine protein kinase that phosphorylates and activates MAPK-kinase (MEK) in response to activation by Ras. ZM 336372 is a potent ATP-competitive inhibitor of Raf-1 in vitro (IC50 = 70 nM) with the paradoxical effect of inducing >100-fold activation of Raf-1 in whole cells. Activation of the Raf-1 signalling pathway using ZM 336372 in human carcinoid tumor cells results in induction of cell cycle inhibitors and suppression of cellular proliferation.
  • Uses It is small molecule tyrosine kinase modulator. It is small molecule tyrosine kinase modulator. ZM336372 induces apoptosis associated with phosphorylation of GSK-3β in pancreatic adenocarcinoma cell lines.
Technology Process of 3-(dimethylamino)-N-(3-(4-hydroxybenzamido)-4-methylphenyl)benzamide

There total 6 articles about 3-(dimethylamino)-N-(3-(4-hydroxybenzamido)-4-methylphenyl)benzamide 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 hydrogen; palladium on activated charcoal; In methanol; at 20 ℃;
DOI:10.1016/j.bmcl.2004.08.006
Guidance literature:
Multi-step reaction with 5 steps
1: (COCl)2; DMF / CH2Cl2 / 20 °C
2: Et3N / CH2Cl2 / 20 °C
3: H2 / Pd/C / methanol / 20 °C
4: Et3N / CH2Cl2 / 20 °C
5: H2 / Pd/C / methanol / 20 °C
With oxalyl dichloride; hydrogen; triethylamine; N,N-dimethyl-formamide; palladium on activated charcoal; In methanol; dichloromethane;
DOI:10.1016/j.bmcl.2004.08.006
Guidance literature:
Multi-step reaction with 4 steps
1: Et3N / CH2Cl2 / 20 °C
2: H2 / Pd/C / methanol / 20 °C
3: Et3N / CH2Cl2 / 20 °C
4: H2 / Pd/C / methanol / 20 °C
With hydrogen; triethylamine; palladium on activated charcoal; In methanol; dichloromethane;
DOI:10.1016/j.bmcl.2004.08.006
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