Welcome to LookChem.com Sign In|Join Free
  • or
(4-OXO-4H-PYRIDIN-1-YL)ACETIC ACID, also known as pyridine-4-carboxylic acid, is a chemical compound with the molecular formula C7H7NO3. It is a derivative of pyridine and a carboxylic acid, making it a common building block in organic synthesis. This versatile compound is characterized by its potential to form various heterocyclic compounds and its utility in the synthesis of pharmaceuticals and agrochemicals.

45965-36-4

Post Buying Request

45965-36-4 Suppliers

Recommended suppliers

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

45965-36-4 Usage

Uses

Used in Pharmaceutical Industry:
(4-OXO-4H-PYRIDIN-1-YL)ACETIC ACID is used as a precursor for the production of various pharmaceuticals, leveraging its ability to be a building block in the synthesis of complex organic molecules. Its presence in the synthesis process contributes to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, (4-OXO-4H-PYRIDIN-1-YL)ACETIC ACID is utilized as a starting material for the synthesis of agrochemicals, such as pesticides and herbicides. Its role in these applications is to provide a foundation for the creation of compounds that can effectively control, repel, or kill pests and weeds in agricultural settings.
Used in Organic Synthesis:
(4-OXO-4H-PYRIDIN-1-YL)ACETIC ACID is used as a key intermediate in organic synthesis for the formation of heterocyclic compounds. Its structural properties allow it to participate in various chemical reactions, leading to the creation of a wide range of organic compounds with diverse applications.
Used as a Chelating Agent:
(4-OXO-4H-PYRIDIN-1-YL)ACETIC ACID has potential applications as a chelating agent, which involves the formation of multiple bonds between a single central atom and a chelating molecule. This property can be harnessed in various chemical processes, including the purification of metal ions and the stabilization of metal complexes.
Used in Supramolecular Chemistry:
In the field of supramolecular chemistry, (4-OXO-4H-PYRIDIN-1-YL)ACETIC ACID is employed in the development of novel materials. Its ability to form complexes and interact with other molecules makes it a valuable component in the design of new materials with unique properties and potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 45965-36-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,5,9,6 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 45965-36:
(7*4)+(6*5)+(5*9)+(4*6)+(3*5)+(2*3)+(1*6)=154
154 % 10 = 4
So 45965-36-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H7NO3/c9-6-1-3-8(4-2-6)5-7(10)11/h1-4H,5H2,(H,10,11)

45965-36-4 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Aldrich

  • (CBR01388)  (4-Oxo-1(4H)-pyridinyl)acetic acid  AldrichCPR

  • 45965-36-4

  • CBR01388-1G

  • 2,255.76CNY

  • Detail

45965-36-4SDS

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 2-(4-oxopyridin-1-yl)acetic acid

1.2 Other means of identification

Product number -
Other names 2-(4-oxohydropyridyl)acetic 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:45965-36-4 SDS

45965-36-4Relevant academic research and scientific papers

7-Acyl-3-(sulfaminoalkyl substituted tetrazolylthiomethyl)cephalosporins, antibacterial compositions containing them and methods of treating bacterial infections with them

-

, (2008/06/13)

The compounds of this invention are cephalosporins having various acyl substituents at the 7-position and a sulfaminoalkyl substituted tetrazolylthiomethyl group at the 3-position of the cephem nucleus and intermediates for the preparation thereof. The 7-acylated cephalosporin compounds have antibacterial activity.

7β-Acylamino-3-(phosphonoalkyl and esterified phosphonoalkyl substituted tetrazolylthiomethyl)cephalosporins

-

, (2008/06/13)

The compounds of this invention are cephalosporins having various acylamino substituents at the 7-position and a phosphonoalkyl or esterified phosphonoalkyl substituted tetrazolylthiomethyl group at the 3-position of the cephem nucleus and intermediates for the preparation thereof. The 7-acylated compounds have antibacterial activity.

7β-Acylamino-3-(alkanesulfonamidoalkyl substituted tetrazolylthiomethyl) cephalosporins, antibacterial compositions containing them and methods of treating bacterial infections with them

-

, (2008/06/13)

The compounds of this invention are cephalosporins having various acyl substituents at the 7-position and an alkanesulfonamidoalkyl substituted tetrazolylthiomethyl group at the 3-position of the cephem nucleus and intermediates for the preparation thereof. The 7-acylated compounds have antibacterial activity.

7-Acyl-3-(carboxyalkyl and carbamoylalkyl substituted oxadiazolylthiomethyl) cephalosporins

-

, (2008/06/13)

The compounds of this invention are cephalosporins having various acyl substituents at the 7-position and a carboxyalkyl or carbamoylalkyl substituted oxadiazolylthiomethyl group at the 3-position of the cephem nucleus and intermediates for the preparation thereof. The 7-acylated compounds have antibacterial activity.

7-Acyl-3-(ureidoalkyl substituted tetrazolylthiomethyl)-cephalosporins

-

, (2008/06/13)

The compounds of this invention are cephalosporins having various acyl substituents at the 7-position and an ureidoalkyl substituted tetrazolylthiomethyl group at the 3-position of the cephem nucleus and intermediates for the preparation thereof. The 7-acylated compounds have antibacterial activity.

4-Oxo-1-pyridinyl penicillin derivatives

-

, (2008/06/13)

Novel substituted(4-oxo-1-pyridinyl)acetylamino-penicillin and cephalosporin derivatives are prepared which are useful antibacterial agents.

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 45965-36-4