Welcome to LookChem.com Sign In|Join Free
  • or
4-[(Pyridin-3-ylcarbonyl)amino]benzoic acid is a chemical compound with the molecular formula C13H10N2O3. It is a derivative of benzoic acid, featuring a pyridine-3-carbonyl group attached to the 4-position of the benzene ring, and an amino group connected to the carbonyl group. 4-[(pyridin-3-ylcarbonyl)amino]benzoic acid is known for its potential applications in the pharmaceutical industry, particularly as a building block for the synthesis of various drugs and medicinal compounds. Its structure allows for the formation of hydrogen bonds and other interactions, which can be crucial for its biological activity. The compound is also of interest in chemical research due to its ability to participate in various chemical reactions, such as condensation and substitution, which can lead to the development of new molecules with specific properties.

5768-40-1

Post Buying Request

5768-40-1 Suppliers

Recommended suppliers

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

5768-40-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5768-40-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,6 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5768-40:
(6*5)+(5*7)+(4*6)+(3*8)+(2*4)+(1*0)=121
121 % 10 = 1
So 5768-40-1 is a valid CAS Registry Number.

5768-40-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(pyridine-3-carbonylamino)benzoic acid

1.2 Other means of identification

Product number -
Other names p-Nicotinamidobenzoic acid

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:5768-40-1 SDS

5768-40-1Relevant academic research and scientific papers

Coordination polymers derived from pyridyl carboxylate ligands having an amide backbone: An attempt towards the selective separation of CuII cation following in situ crystallization under competitive conditions

Paul, Mithun,Dastidar, Parthasarathi

, p. 7815 - 7829 (2014/08/18)

A series of coordination polymers (CPs) derived from pyridyl carboxylate ligands equipped with a hydrogen bonding backbone (amide), namely L1 [sodium 4-(nicotinamido) benzoate] and L2 [sodium 3-(nicotinamido) benzoate], has been synthesized and characterized by single crystal X-ray diffraction. The effect of the ligating topology of these two positional isomers (L1 and L2) on the resultant supramolecular architecture of the corresponding CPs was investigated. The results indicate that most of the CPs display a 1D looped chain topology. Following in situ crystallization technique, attempts were made to separate environmentally toxic metal cation CuII in the form of the corresponding CuII CPs from a complex mixture of cations (Cu II, ZnII and CoII) using both the ligands, while L1 was unsuccessful, L2 could indeed separate the CuII cation. The coordinating ability of the pyridyl and carboxylate moieties on the selective separation of cations was investigated. The results indicate that the selective separation of CuII followed the Irving-Williams series. Atomic absorption spectroscopy revealed that ~97% of CuII could be separated by this technique.

QSAR study on antibacterial activity of sulphonamides and derived Mannich bases

Joshi, Sheela,Khosla, Navita

, p. 3747 - 3751 (2007/10/03)

The paper describes synthesis and comparative study on antibacterial activities of sulphonamides and Mannich bases derived from them. The compounds were screened for their antibacterial activity against various gram-positive and gram-negative bacteria and were analyzed statistically. The results have shown that the compounds are quiet active against pathogens under study and were nontoxic.

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 5768-40-1