1298044-15-1

Basic information

• Product Name: (E)-3-(6-bromo-2-chloroquinolin-3-yl)prop-2-en-1-ol
• Synonyms: (E)-3-(6-bromo-2-chloroquinolin-3-yl)prop-2-en-1-ol
• CAS NO: 1298044-15-1
• Molecular Weight: 298.567
• Mol File: 1298044-15-1.mol
• Article Data: 0

Chemical Properties

• CAS DataBase Reference: (E)-3-(6-bromo-2-chloroquinolin-3-yl)prop-2-en-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-3-(6-bromo-2-chloroquinolin-3-yl)prop-2-en-1-ol(1298044-15-1)
• EPA Substance Registry System: (E)-3-(6-bromo-2-chloroquinolin-3-yl)prop-2-en-1-ol(1298044-15-1)

Safety Data

• Hazardous Substances Data: 1298044-15-1(Hazardous Substances Data)

Usage

Description

(E)-3-(6-bromo-2-chloroquinolin-3-yl)prop-2-en-1-ol is a chemical compound with a molecular formula C13H8BrClNO. It is a derivative of quinoline, a heterocyclic aromatic compound. (E)-3-(6-bromo-2-chloroquinolin-3-yl)prop-2-en-1-ol contains a hydroxyl group and a double bond, giving it both alcohol and alkene functionalities. Its structure includes a quinoline ring with bromine and chlorine substituents, as well as a propenol side chain. Due to its unique structure and properties, (E)-3-(6-bromo-2-chloroquinolin-3-yl)prop-2-en-1-ol may have potential applications in various fields such as pharmaceuticals, agrochemicals, or material science. However, further research and testing are required to fully understand its applications and potential uses.

Uses

Used in Pharmaceutical Industry:
(E)-3-(6-bromo-2-chloroquinolin-3-yl)prop-2-en-1-ol is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure, which includes a quinoline ring with bromine and chlorine substituents, may contribute to the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, (E)-3-(6-bromo-2-chloroquinolin-3-yl)prop-2-en-1-ol may be used as a building block for the development of novel agrochemicals, such as pesticides or herbicides. Its chemical properties, including the presence of a hydroxyl group and a double bond, could be exploited to create new molecules with improved efficacy and selectivity.
Used in Material Science:
(E)-3-(6-bromo-2-chloroquinolin-3-yl)prop-2-en-1-ol may also find applications in the field of material science. Its quinoline-based structure and functional groups could be utilized in the design and synthesis of new materials with specific properties, such as optoelectronic materials, sensors, or advanced polymers.

Downstream Products

• 1298044-24-2 (2R)-2-(6-bromo-2-methoxyquinolin-3-yl)-1-(naphthalen-1-yl)-2-phenylethanol 
• 1298044-21-9 C₁₈H₁₄BrNO₂ 
• 1298044-19-5 (2R,3R)-3-(6-bromo-2-methoxyquinolin-3-yl)-3-phenylpropane-1,2-diol 
• 1298044-33-3 (4R)-4-(6-bromo-2-methoxyquinolin-3-yl)-3-hydroxy-3-(naphthalen-1-yl)-4-phenylbutyl methanesulfonate 
• 1298044-31-1 (4R)-4-(6-bromo-2-methoxyquinolin-3-yl)-3-(naphthalen-1-yl)-4-phenylbutane-1,3-diol 
• 1298044-29-7 C₃₀H₂₄BrNO₃ 
• 1298044-27-5 (1R)-1-(6-bromo-2-methoxyquinolin-3-yl)-2-(naphthalen-1-yl)-1-phenylpent-4-en-2-ol 
• 1298044-25-3 (2R)-2-(6-bromo-2-methoxyquinolin-3-yl)-1-(naphthalen-1-yl)-2-phenylethanone 
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• 857086-94-3 (1R,2R)-1-(6-bromo-2-methoxyquinolin-3-yl)-4-(dimethylamino)-2-(naphthalen-1-yl)-1-phenylbutan-2-ol