887580-55-4

Basic information

• Product Name: 2-CHLOROL-4-PYRIDINE ACETIC ACID
• Synonyms: 2-CHLOROL-4-PYRIDINE ACETIC ACID;(2-CHLORO-PYRIDIN-4-YL)-ACETIC ACID;2-Chloro-4-pyridineacetic acid;2-Chloropyridine-4-acetic acid;2-Chloropyridine-4-acetic acid 97%;2-(2-chloropyridin-4-yl)acetic acid
• CAS NO: 887580-55-4
• Molecular Formula: C₇H₆ClNO₂
• Molecular Weight: 171.58
• Mol File: 887580-55-4.mol

Chemical Properties

• Melting Point: 140-145°C
• Boiling Point: 338.8°C at 760 mmHg
• Flash Point: 158.7°C
• Appearance: /
• Density: 1.405g/cm³
• Vapor Pressure: 3.74E-05mmHg at 25°C
• Refractive Index: 1.575
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 3.66±0.10(Predicted)
• CAS DataBase Reference: 2-CHLOROL-4-PYRIDINE ACETIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2-CHLOROL-4-PYRIDINE ACETIC ACID(887580-55-4)
• EPA Substance Registry System: 2-CHLOROL-4-PYRIDINE ACETIC ACID(887580-55-4)

Safety Data

• Hazard Codes: Xn
• Statements: 22-36/37/38
• Safety Statements: 26
• WGK Germany: 3
• Hazardous Substances Data: 887580-55-4(Hazardous Substances Data)

Usage

Uses

Used in Agricultural Industry:
2-Chloro-4-pyridine acetic acid is used as a herbicidal agent for controlling broadleaf weeds in various crops. It is applied to selectively target and eliminate unwanted plant species, thereby promoting the growth and health of the intended crops. Its use in agriculture is valued for its effectiveness in managing weed populations without causing damage to the cultivated plants.
Used in Residential Weed Control:
In addition to its agricultural applications, 2-Chloro-4-pyridine acetic acid can also be found in residential weed control products. It serves as an effective solution for homeowners and gardeners to manage and eliminate unwanted broadleaf weeds in their gardens and lawns, ensuring a clean and well-maintained outdoor space.
However, it is crucial to exercise caution when using 2-Chloro-4-pyridine acetic acid, as it has been identified as potentially toxic to aquatic organisms. Additionally, there is a risk of this chemical leaching into groundwater, which necessitates responsible and careful application to minimize environmental impact.

InChI:InChI=1/C7H6ClNO2/c8-6-3-5(1-2-9-6)4-7(10)11/h1-3H,4H2,(H,10,11)

Upstream product

• 3678-62-4 2-chloro-4-picoline 
• 937236-73-2 ethyl 2-(2-chloropyridin-4-yl)acetate 
• 896107-40-7 diethyl 2-(2-chloro-4-pyridinyl)malonate 

Downstream Products

• 1333468-83-9 1-(4-methylpiperazin-1-yl)-2-(2-(4-methylpiperazin-1-yl)pyridin-4-yl)ethanone 
• 1256825-57-6 2-(2-(4-methylpiperazin-1-yl)pyridin-4-yl)acetic acid 
• 1333468-84-0 methyl 2-(2-(4-methylpiperazin-1-yl)pyridin-4-yl)acetate 
• 860468-72-0 2-(2-(4-methylpiperazin-1-yl)pyridin-4-yl)acetamide 
• 860468-74-2 tert-butyl 2-(2-chloropyridin-4-yl)acetate 

Relevant articles and documents

LABELLED COUMARIN DERIVATIVES

The present invention relates to compounds having selective binding for MAO-B as compared with MAO-A. The invention also provides radioactive versions of these compounds, and precursor compounds for the synthesis of these radioactive compounds. The radioactive compounds of the invention can find use for in vivo imaging applications.

Inhibitors of protein kinases

Compounds of general Formula (I): wherein R1, R2, R3, Ra, A, B and x are as defined herein are inhibitors of protein kinases in particular members of the cyclin-dependent kinase family and/or the glycogen synthase kinase 3 family and are useful in preventing and/or treating any type of pain, inflammatory disorders, cancer, immunological diseases, proliferative diseases, infectious diseases, cardiovascular diseases, metabolic disorders, renal diseases, neurologic and neuropsychiatric diseases and neurodegenerative diseases.

BETA-LACTAMASE INHIBITORS

Disclosed herein are α-aminoboronic acids and their derivatives which act as inhibitors of beta-lactamases. Also disclosed herein are pharmaceutical compositions comprising α-aminoboronic acids and methods of use thereof.