Welcome to LookChem.com Sign In|Join Free

CAS

  • or

13025-99-5

Post Buying Request

13025-99-5 Suppliers

Recommended suppliersmore

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

13025-99-5 Usage

General Description

N-[(E)-4-pyridylmethyleneamino]pyridine-4-carboxamide is a chemical compound with the molecular formula C13H10N4O. It is a derivative of pyridine and contains an amide group. N-[(E)-4-pyridylmethyleneamino]pyridine-4-carboxamide may have potential applications in the field of pharmaceuticals due to its structure, which may allow for interactions with biological systems. Additionally, its properties may make it useful for research purposes in the study of organic chemistry and drug development. Further research is needed to fully understand the potential uses and properties of N-[(E)-4-pyridylmethyleneamino]pyridine-4-carboxamide.

Check Digit Verification of cas no

The CAS Registry Mumber 13025-99-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,2 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13025-99:
(7*1)+(6*3)+(5*0)+(4*2)+(3*5)+(2*9)+(1*9)=75
75 % 10 = 5
So 13025-99-5 is a valid CAS Registry Number.

13025-99-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(E)-pyridin-4-ylmethylideneamino]pyridine-4-carboxamide

1.2 Other means of identification

Product number -
Other names pyridine-4-carboxaldehyde isonicotinoyl hydrazone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13025-99-5 SDS

13025-99-5Downstream Products

13025-99-5Relevant articles and documents

Isonicotinohydrazones as inhibitors of alkaline phosphatase and ecto-5′-nucleotidase

Channar, Pervaiz Ali,Shah, Syed Jawad Ali,Hassan, Sidra,Nisa, Zaib un,Lecka, Joanna,Sévigny, Jean,Bajorath, Jürgen,Saeed, Aamer,Iqbal, Jamshed

, p. 365 - 370 (2017)

A series of isonicotinohydrazide derivatives was synthesized and tested against recombinant human and rat ecto-5′-nucleotidases (h-e5′NT and r-e5′NT) and alkaline phosphatase isozymes including both bovine tissue-non-specific alkaline phosphatase (b-TNAP)

A novel dicationic ionic liquids encompassing pyridinium hydrazone-phenoxy conjugates as antimicrobial agents targeting diverse high resistant microbial strains

Rezki, Nadjet,Al-Sodies, Salsabeel A.,Ahmed, Hany E.A.,Ihmaid, Saleh,Messali, Mouslim,Ahmed, Sahar,Aouad, Mohamed Reda

, p. 431 - 444 (2019)

A focused library of new dicationic ionic liquids (DiILs) 6–41 appended pyridinium hydrazone and phenoxy side chain hybrids as counter cations were designed and synthesized, utilizing quaternization and metathesis reactions under both conventional and microwave irradiation. The novel DiILs 6–41 were fully characterized using different spectroscopic tools (1H, 13C, 19F, 11B, 31P NMR and mass spectra) and evaluated for their antimicrobial activity against diverse types of high resistant strains including two Gram-positive bacteria; methicillin-resistant Staphylococcus aureus (MRSA), Clostridium difficile, two Gram-negative bacteria; two Escherichia coli isolates, and Neisseria gonorrhea, and fungal strain; Candida albicans. The antibacterial screening was carried out by broth microdilution method and MIC values were reported as indicator of growth inhibition. They mostly exhibited antibacterial effect against MRSA and EC strains. The effect of the synthesized ILs on Gram-positive bacteria showed the phenoxy linker chain increases, the MIC values increases with more lethal effect due to the hydrophobicity parameter. This behavior was confirmed by the molecular dynamic simulation through the interaction with surface membrane as general mechanism of ILs. The dicationic ionic liquids are considered promising motifs for further investigations with focusing on the terminal hydrophobic adjuster.

pH-Induced formation of metalloligand: Increasing structure dimensionality by tuning number of ligand functional sites

Ni, Wen-Xiu,Li, Mian,Zhou, Xiao-Ping,Li, Zhen,Huang, Xiao-Chun,Li, Dan

, p. 3479 - 3481 (2007)

Two complexes, 2D [Cu2(CN)2(4-Hpcih)]n and 3D {[Cu2(CN)1.5(4-pcih)]·1.25H2O} n (4-Hpcih = 4-pyridinecarbaldehyde isonicotinoyl hydrazone), were obtained using a synthetic approach of pH-induced formation of metalloligands, successfully demonstrating a strategy to increase structure dimensionality by tuning the number of ligand functional sites. The Royal Society of Chemistry.

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

What can I do for you?
Get Best Price

Get Best Price for 13025-99-5