1298044-27-5

Usage

Uses

Used in Pharmaceutical Industry:
(1R)-1-(6-bromo-2-methoxyquinolin-3-yl)-2-(naphthalen-1-yl)-1-phenylpent-4-en-2-ol is used as a potential candidate for drug development due to its complex structure and unique functional groups. Its specific molecular properties may allow it to interact with biological targets in ways that could lead to the development of new therapeutic agents.
Used in Materials Science:
In the field of materials science, (1R)-1-(6-bromo-2-methoxyquinolin-3-yl)-2-(naphthalen-1-yl)-1-phenylpent-4-en-2-ol may be utilized for the creation of new materials with specialized properties. Its structural components could contribute to the development of advanced materials with applications in various industries, such as electronics, coatings, or composites.
Further research and exploration of the chemical and biological properties of (1R)-1-(6-bromo-2-methoxyquinolin-3-yl)-2-(naphthalen-1-yl)-1-phenylpent-4-en-2-ol will be necessary to fully understand its potential and unlock its applications across different industries.

Upstream product

• 1298044-25-3 (2R)-2-(6-bromo-2-methoxyquinolin-3-yl)-1-(naphthalen-1-yl)-2-phenylethanone 
• 18925-10-5 allylzinc bromide 
• 1298044-13-9 ethyl (E)-3-(6-bromo-2-chloroquinolin-3-yl)acrylate 
• 1298044-15-1 (E)-3-(6-bromo-2-chloroquinolin-3-yl)prop-2-en-1-ol 
• 1298044-17-3 (E)-3-(6-bromo-2-methoxyquinolin-3-yl)prop-2-en-1-ol 
• 1298044-10-6 [(2S,3S)-3-(6-bromo-2-methoxyquinolin-3-yl)oxiran-2-yl]methanol 
• 1298044-19-5 (2R,3R)-3-(6-bromo-2-methoxyquinolin-3-yl)-3-phenylpropane-1,2-diol 
• 1298044-21-9 C₁₈H₁₄BrNO₂ 
• 73568-35-1 6-bromo-2-chloro-3-formylquinoline 

Downstream Products

• 843663-66-1 bedaquiline 
• 857086-94-3 (1R,2R)-1-(6-bromo-2-methoxyquinolin-3-yl)-4-(dimethylamino)-2-(naphthalen-1-yl)-1-phenylbutan-2-ol 
• 1298044-29-7 C₃₀H₂₄BrNO₃ 
• 1298044-31-1 (4R)-4-(6-bromo-2-methoxyquinolin-3-yl)-3-(naphthalen-1-yl)-4-phenylbutane-1,3-diol 
• 1298044-33-3 (4R)-4-(6-bromo-2-methoxyquinolin-3-yl)-3-hydroxy-3-(naphthalen-1-yl)-4-phenylbutyl methanesulfonate 

Relevant academic research and scientific papers

Practical syntheses of (2S)-R207910 and (2R)-R207910

Concise and practical syntheses of (2S)-R207910 (3a) and (2R)-R207910 (3b) have been achieved in high overall yield of 12 % in 10 steps for each isomer starting from a known intermediate following Sharpless asymmetric epoxidation, regioselective epoxide opening, modified allylzinc bromide addition as key reactions. Copyright