474707-27-2

Basic information

• Product Name: 1-(6-bromo-4-quinolyl)-4-piperidyl methyl ether
• Synonyms: 1-(6-bromo-4-quinolyl)-4-piperidyl methyl ether
• CAS NO: 474707-27-2
• Molecular Weight: 321.217
• Mol File: 474707-27-2.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 441.5±45.0 °C(Predicted)
• Density: 1.44±0.1 g/cm3(Predicted)
• CAS DataBase Reference: 1-(6-bromo-4-quinolyl)-4-piperidyl methyl ether(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(6-bromo-4-quinolyl)-4-piperidyl methyl ether(474707-27-2)
• EPA Substance Registry System: 1-(6-bromo-4-quinolyl)-4-piperidyl methyl ether(474707-27-2)

Safety Data

• Hazardous Substances Data: 474707-27-2(Hazardous Substances Data)

Usage

Description

1-(6-bromo-4-quinolyl)-4-piperidyl methyl ether is a synthetic chemical compound with the formula C17H18BrN3O. It is often utilized as an intermediate in the production of pharmaceuticals and agrochemicals due to its biological activity, particularly as an inhibitor of certain enzymes. 1-(6-bromo-4-quinolyl)-4-piperidyl methyl ether should be handled with care, as it may possess toxic or irritant properties, and further research is required to fully comprehend its potential applications and risks.

Uses

Used in Pharmaceutical Industry:
1-(6-bromo-4-quinolyl)-4-piperidyl methyl ether is used as an intermediate compound for the synthesis of various pharmaceuticals. Its biological activity as an enzyme inhibitor makes it a valuable component in the development of drugs targeting specific enzyme-related conditions.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(6-bromo-4-quinolyl)-4-piperidyl methyl ether is employed as an intermediate in the production of agrochemicals. Its role in inhibiting certain enzymes can be leveraged to create products that address specific needs in agriculture, such as pest control or crop protection.

Upstream product

• 65340-70-7 6-bromo-4-chloroquinoline 
• 4045-25-4 4-methoxypiperidine hydrochloride 

Downstream Products

• 1201842-73-0 N-(2-chloro-5-(4-(4-methoxy-1-piperidinyl)-6-quinolinyl)-3-pyridinyl)-4-methoxybenzenesulfonamide 

Relevant articles and documents

NITROGENOUS FUSED?RING COMPOUND HAVING PYRAZOLYL GROUP AS SUBSTITUENT AND MEDICINAL COMPOSITION THEREOF

The present invention provides a compound having an excellent inhibitory action on activation of STAT6 and a pharmaceutical composition thereof. Inparticular, it provides a compound represented by the following formula (I), a salt thereof or a hydrate of them. In the formula, X represents a nitrogen-containing condensed aromatic heterocyclic group such as imidazo[1,2-a]pyridine, benzimidazole, quinazoline, quinoline, or 2,1-benzisoxazole and has (R4)n as substituent groups; Y represents a C3-8 cycloalkyl group, C4-8 cycloalkenyl group, 5- to 14-membered non-aromatic heterocyclic group, C6-14 aromatic hydrocarbon cyclic group or 5- to 14-membered aromatic heterocyclic group; n in (R4)n is 0, 1, 2 or 3, and Z groups independently represent (1) hydrogen atom, (2) amino group, (3) halogen atom, (4) hydroxyl group, (5) nitro group, (6) cyano group, (7) azido group, (8) formyl group, (9) hydroxyamino group, (10) sulfamoyl group, (11) guanodino group, (12) oxo group, (13) C2-6 alkenyl group, (14) C1-6 alkoxy group, (15) C1-6 alkylhydroxyamino group, (16) halogenated C1-6 alkyl group, (17) halogenated C2-6 alkenyl group, (18) (i) C3-7cycloalkyl group, (ii) C3-7cycloalkenyl group, (iii) 5- to 14-membered non-aromatic heterocyclic group, each of which may have one or more substituent groups Q, or (19) formula -M1-M2-M3, R1 represents (1) hydrogen atom, (2) halogen atom, (3) hydroxyl group, (4) nitro group, (5) cyano group, (6) halogenated C1-6 alkyl group, (7) C2-6 alkyl group substituted with a hydroxyl or cyano group, (8) C2-6 alkenyl group, or (9) formula -L1-L2-L3, and R2 represents a hydrogen atom or a protecting group; and R3 represents a hydrogen atom, halogen atom, cyano group, amino group, C1-4 alkyl group or halogenated C1-4 alkyl group.