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(2R,3R)-3-(6-bromo-2-methoxyquinolin-3-yl)-3-phenylpropane-1,2-diol is a complex chemical compound characterized by its unique structure that includes a quinoline ring, a phenyl group, and a diol moiety. The "2R,3R" notation signifies the presence of two chiral centers with specific stereochemistry, which is crucial for its potential biological activities. The bromine and methoxy substituents on the quinoline ring, along with the phenyl group, contribute to the compound's distinctive properties. The diol functionality suggests possible interactions with biological systems, making it a promising candidate for drug discovery or medicinal chemistry. (2R,3R)-3-(6-bromo-2-methoxyquinolin-3-yl)-3-phenylpropane-1,2-diol's specific structural features and stereochemistry render it an intriguing target for further research and potential applications in pharmaceutical research.

1298044-19-5

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1298044-19-5 Usage

Uses

Used in Pharmaceutical Research:
(2R,3R)-3-(6-bromo-2-methoxyquinolin-3-yl)-3-phenylpropane-1,2-diol is utilized as a research compound for exploring its potential biological activities and interactions with biological systems. Its unique structure and stereochemistry make it a valuable tool in drug discovery, where it can be further studied and optimized for specific therapeutic applications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (2R,3R)-3-(6-bromo-2-methoxyquinolin-3-yl)-3-phenylpropane-1,2-diol serves as a starting point for the development of new pharmaceutical agents. Its structural features and diol functionality can be leveraged to design and synthesize novel compounds with improved pharmacological properties, such as enhanced potency, selectivity, and reduced side effects.
Used in Drug Discovery:
(2R,3R)-3-(6-bromo-2-methoxyquinolin-3-yl)-3-phenylpropane-1,2-diol is employed as a lead compound in drug discovery efforts. Its complex structure and potential interactions with biological targets make it a promising candidate for the development of new therapeutic agents. Researchers can use (2R,3R)-3-(6-bromo-2-methoxyquinolin-3-yl)-3-phenylpropane-1,2-diol as a basis for designing and testing new drugs with specific pharmacological profiles and therapeutic indications.
Used in Chemical Synthesis:
In the realm of chemical synthesis, (2R,3R)-3-(6-bromo-2-methoxyquinolin-3-yl)-3-phenylpropane-1,2-diol can be used as a building block or intermediate in the synthesis of more complex molecules. Its unique structural features and functional groups can be exploited to create new compounds with diverse applications in various fields, including materials science, agrochemicals, and specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 1298044-19-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,8,0,4 and 4 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1298044-19:
(9*1)+(8*2)+(7*9)+(6*8)+(5*0)+(4*4)+(3*4)+(2*1)+(1*9)=175
175 % 10 = 5
So 1298044-19-5 is a valid CAS Registry Number.

1298044-19-5Relevant academic research and scientific papers

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

Chandrasekhar, Srivari,Babu, G. S. Kiran,Mohapatra, Debendra K.

, p. 2057 - 2061 (2011)

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

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