Welcome to LookChem.com Sign In|Join Free
  • or
Benzoic acid, 3-[(2-pyridinylmethylene)amino]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

42974-36-7

Post Buying Request

42974-36-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

42974-36-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42974-36-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,9,7 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 42974-36:
(7*4)+(6*2)+(5*9)+(4*7)+(3*4)+(2*3)+(1*6)=137
137 % 10 = 7
So 42974-36-7 is a valid CAS Registry Number.

42974-36-7Relevant academic research and scientific papers

Synthesis, Characterization, and Magnetic Properties of a Series of Copper(II) Chloride Complexes of Pyridyliminebenzoic Acids

Buvaylo, Elena A.,Kokozay, Vladimir N.,Makhankova, Valeriya G.,Melnyk, Andrii K.,Korabik, Maria,Witwicki, Maciej,Skelton, Brian W.,Vassilyeva, Olga Yu.

, p. 1603 - 1619 (2018)

A series of CuII halide complexes, Cu(HL1)Cl2·CH3OH (1), [Cu(L1)Cl]2·H2O (2), [Cu(HL2)Cl2]2·2DMF (3), [Cu(HL2)2Cl]nCln·2nH2O (4), and

Synthesis, Structure and Cytotoxicity of N,N and N,O-Coordinated RuII Complexes of 3-Aminobenzoate Schiff Bases against Triple-negative Breast Cancer

Mukherjee, Arpan,Koley, Tuhin Subhra,Chakraborty, Ayan,Purkait, Kallol,Mukherjee, Arindam

, p. 3729 - 3742 (2021/10/14)

Half-sandwich RuII complexes, [(YZ)RuII(η6-arene)(X)]+, (YZ=chelating bidentate ligand, X=halide), with N,N and N,O coordination (1–9) show significant antiproliferative activity against the metastatic triple-negative breast carcinoma (MDA-MB-231). 3-aminobenzoic acid or its methyl ester is used in all the ligands while varying the aldehyde for N,N and N,O coordination. In the N,N coordinated complex the coordinated halide(X) is varied for enhancing stability in solution (X=Cl, I). Rapid aquation and halide exchange of the pyridine analogues, 2 and 3, in solution are a major bane towards their antiproliferative activity. Presence of free ?COOH group (1 and 4) make complexes hydrophilic and reduces toxicity. The imidazolyl 3-aminobenzoate based N,N coordinated 5 and 6 display better solution stability and efficient antiproliferative activity (IC50 ca. 2.3–2.5 μM) compared to the pyridine based 2 and 3 (IC50>100 μM) or the N,O coordinated complexes (7–9) (IC50 ca. 7–10 μM). The iodido coordinated, 6, is resistant towards aquation and halide exchange. The N,O coordinated 7–9 underwent instantaneous aquation at pH 7.4 generating monoaquated complexes stable for at least 6 h. Complexes 5 and 6, bind to 9-ethylguanine (9-EtG) showing propensity to interact with DNA bases. The complexes may kill via apoptosis as displayed from the study of 8. The change in coordination mode and the aldehyde affected the solution stability, antiproliferative activity and mechanistic pathways. The N,N coordinated (5 and 6) exhibit arrest in the G2/M phase while the N,O coordinated 8 showed arrest in the G0/G1 phase.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 42974-36-7