84596-08-7

Basic information

• Product Name: 2-Pyridinamine, 5-(4-chlorophenyl)-
• Synonyms: 5-(4-chlorophenyl)pyridin-2-ylamine;5-(4-chlorophenyl)pyridin-2-aMine;2-Pyridinamine, 5-(4-chlorophenyl)-
• CAS NO: 84596-08-7
• Molecular Formula: C₁₁H₉ClN₂
• Molecular Weight: 205
• Mol File: 84596-08-7.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 352℃
• Flash Point: 167℃
• Appearance: /
• Density: 1.261
• Storage Temp.: 2-8°C(protect from light)
• CAS DataBase Reference: 2-Pyridinamine, 5-(4-chlorophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Pyridinamine, 5-(4-chlorophenyl)-(84596-08-7)
• EPA Substance Registry System: 2-Pyridinamine, 5-(4-chlorophenyl)-(84596-08-7)

Safety Data

• Hazardous Substances Data: 84596-08-7(Hazardous Substances Data)

Usage

General Description

2-Pyridinamine, 5-(4-chlorophenyl)- is a chemical compound with the molecular formula C11H9ClN2. It is a derivative of pyridine and contains a chlorophenyl group. 2-Pyridinamine, 5-(4-chlorophenyl)- is primarily used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It may also have potential industrial uses as a building block in the production of various organic compounds. 2-Pyridinamine, 5-(4-chlorophenyl)- should be handled and used with caution, as it may pose health and environmental risks if not properly managed.

Upstream product

• 1072-97-5 5-bromo-2-pyridylamine 
• 1679-18-1 4-Chlorophenylboronic acid 
• 96042-30-7 4-(dicyanomethylene)-2-methyl-6-(p-dimethylaminostyryl)-4H-pyran 
• 274251-56-8 boronic acid 4-chlorophenyl monoester 

Downstream Products

• 84596-52-1 5-(4-chlorophenyl)-2-pyridylamine-1-oxide 
• 690264-18-7 5-(4-chloro-phenyl)-2-iodo-pyridine 
• 1044239-23-7 N-[5-(4-chlorophenyl)pyridin-2-yl]benzamide 
• 918516-27-5 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine 
• 1029872-54-5 vemurafenib 
• 911113-60-5 C₁₁H₈BrClN₂ 
• 1356397-47-1 C₁₅H₁₅ClN₂O 
• 1356397-48-2 5-(4-Cl-phenyl)azaindole 
• 1356397-46-0 C₁₁H₈ClIN₂ 

Relevant articles and documents

Imidazo[1,2- a]pyridine derivatives as aldehyde dehydrogenase inhibitors: Novel chemotypes to target glioblastoma stem cells

Glioblastoma multiforme (GBM) is the deadliest form of brain tumor. It is known for its ability to escape the therapeutic options available to date thanks to the presence of a subset of cells endowed with stem-like properties and ability to resist to cyto

NOVEL PROCESSES FOR THE MANUFACTURE OF PROPANE-1-SULFONIC ACID {3-[5-(4-CHLORO-PHENYL)-1H-PYRROLO[2,3-B]PYRIDINE-3-CARBONYL]-2,4-DIFLUORO-PHENYL}-AMIDE

According to the present invention there are provided novel processes for the manufacture of the compound of formula (1) as well as novel synthesis routes for key intermediates used in those processes.

Novel compounds as metabotropic glutamate receptor antagonists

The present invention relates to compounds of formula (I) wherein A, E G, J, L, M, R1, R2, and R3 are as defined in the specification and claims. The invention also relates to pharmaceutical compositions containing such compounds and methods for preparing the compounds and compositions. The compounds are metabotropic glutamate receptor antagonists and are useful for the treatment of a variety of CNS disorders.