79205-04-2

Basic information

• Product Name: 2-Methyl-5-Methoxyquinoline
• Synonyms: 2-Methyl-5-Methoxyquinoline;5-Methoxy-2-Methylquinoline
• CAS NO: 79205-04-2
• Molecular Formula: C₁₁H₁₁NO
• Molecular Weight: 173.21114
• EINECS: -0
• Mol File: 79205-04-2.mol
• Article Data: 11

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-Methyl-5-Methoxyquinoline(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Methyl-5-Methoxyquinoline(79205-04-2)
• EPA Substance Registry System: 2-Methyl-5-Methoxyquinoline(79205-04-2)

Safety Data

• Hazardous Substances Data: 79205-04-2(Hazardous Substances Data)

Usage

General Description

2-Methyl-5-Methoxyquinoline is a chemical compound with the molecular formula C11H11NO. It is a derivative of quinoline, an aromatic compound commonly found in certain types of plants. The compound is known for its yellowish-brown color and has been used in various industrial and research applications. It is also known to have potential biological activity and may be of interest in the development of pharmaceuticals and other compounds with medicinal properties. Additionally, 2-Methyl-5-Methoxyquinoline is used as a building block in organic synthesis and has been studied for its potential as an antioxidant and for other antioxidant-related effects.

Upstream product

• 54408-52-5 5-bromo-2-methylquinoline 
• 123-73-9 trans-Crotonaldehyde 
• 536-90-3 m-Anisidine 
• 123-73-9 crotonaldehyde 
• 54408-50-3 2-methyl-5-aminoquinoline 
• 23877-94-3 2-methyl-5-nitroquinoline 
• 57155-51-8 2-Methyl-quinoline-5-diazonium; bromide 
• 64-17-5 ethanol 
• 90-04-0 2-methoxy-phenylamine 
• 2401-24-3 2-chloro-5-methoxyaniline 

Downstream Products

• 852402-70-1 5-methoxyquinoline-2-carboxylic acid 
• 852402-73-4 (S)-5-methoxyquinoline-2-carboxylic acid (1-phenylethyl)amide 
• 852402-83-6 (2S,3'S)-5-methoxy-1,2,3,4-tetrahydroquinoline-2-carboxylic acid (1-phenylethyl)amide 
• 852402-78-9 (2R,3'S)-5-methoxy-1,2,3,4-tetrahydroquinoline-2-carboxylic acid (1-phenylethyl)amide 
• 852402-99-4 (4aR,1'S)-7-methoxy-3-(1-phenylethyl)-2,3,4,4a,5,6-hexahydro-1H-pyrazino[1,2-a]quinoline 
• 852403-04-4 (4aS,1'S)-7-methoxy-3-(1-phenylethyl)-2,3,4,4a,5,6-hexahydro-1H-pyrazino[1,2-a]quinoline 
• 852402-89-2 (4aR,1'S)-7-methoxy-3-(1-phenylethyl)-2,3,4,4a,5,6-hexahydropyrazino[1,2-a]quinolin-1-one 
• 852402-94-9 (4aS,1'S)-7-methoxy-3-(1-phenylethyl)-2,3,4,4a,5,6-hexahydropyrazino[1,2-a]quinolin-1-one 
• 1422841-39-1 C₂₆H₂₂N₄O₂ 
• 1422841-62-0 C₂₆H₂₂N₄O₂ 

Relevant articles and documents

BROMODOMAIN INHIBITORS FOR ANDROGEN RECEPTOR-DRIVEN CANCERS

Methods for treating certain androgen receptor-positive forms of cancer using inhibitors of the CREB binding protein bromodomain are disclosed. In some methods, the AR-positive forms of cancer may be breast cancer, including triple negative forms, hormone receptor positive forms, and HER2-positive forms. In other methods, the AR-positive forms of cancer may be prostate cancer, including metastatic castration resistant prostate cancer. In some embodiments, methods of treating prostate cancer comprise the step of administering to a patient in need thereof the compound (1R,3R)-3-[(7S)-2-[(R)-(5-fluoro-2-methoxyphenyl)(hydroxy)methyl]-6-(methoxycarbonyl)-7-methyl-3H,6H,7H,8H,9H-imidazo[4,5-f]quinolin-3-yl]cyclohexane-1-carboxylic acid, or a pharmaceutically acceptable salt thereof.

Rapid Construction of Structurally Diverse Quinolizidines, Indolizidines, and Their Analogues via Ruthenium-Catalyzed Asymmetric Cascade Hydrogenation/Reductive Amination

A rapid construction of enantioenriched benzo-fused quinolizidines, indolizidines, and their analogues by ruthenium-catalyzed asymmetric cascade hydrogenation/reductive amination of quinolinyl- and quinoxalinyl-containing ketones has been developed. This

TETRAHYDROQUINOLINE COMPOSITIONS AS BET BROMODOMAIN INHIBITORS

The present invention relates to inhibitors of bromo and extra terminal (BET) bromodomains that are useful for the treatment of cancer, inflammatory diseases, diabetes, and obesity, having Formula (I): wherein W, X, Y, Z, R1, R2, R5, and R8 are as described herein.