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1315508-96-3

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1315508-96-3 Usage

Description

(S)-2-chloro-1-((S)-6-fluoro-3,4-dihydro-2H-chromen-2-yl)ethanol is a complex chiral chemical compound characterized by the presence of chloro, fluoro, ethanol, and chromen-2-yl functional groups. This molecule features two stereocenters, which contribute to its unique structure and properties. Its specific optical rotation and the potential for various interactions due to its functional groups make it a compound of interest, particularly in the field of medicinal chemistry.

Uses

Used in Pharmaceutical Development:
(S)-2-chloro-1-((S)-6-fluoro-3,4-dihydro-2H-chromen-2-yl)ethanol is used as a key intermediate in the pharmaceutical industry for the development of new drugs. Its unique structure and properties allow for the creation of novel therapeutic agents that can potentially target a wide range of medical conditions.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (S)-2-chloro-1-((S)-6-fluoro-3,4-dihydro-2H-chromen-2-yl)ethanol serves as a valuable compound for research purposes. Its specific functional groups and stereochemistry make it an ideal candidate for studying the effects of molecular structure on biological activity, which can lead to the discovery of new pharmaceuticals with improved efficacy and selectivity.
Used in Drug Design and Optimization:
(S)-2-chloro-1-((S)-6-fluoro-3,4-dihydro-2H-chromen-2-yl)ethanol is used as a building block in drug design and optimization processes. Its unique functional groups can be modified or combined with other molecules to create new drug candidates with enhanced properties, such as increased potency, improved pharmacokinetics, or reduced side effects.
Used in Chiral Synthesis:
Due to its chiral nature and two stereocenters, (S)-2-chloro-1-((S)-6-fluoro-3,4-dihydro-2H-chromen-2-yl)ethanol is used in chiral synthesis, which is crucial for the development of enantiomerically pure drugs. (S)-2-chloro-1-((S)-6-fluoro-3,4-dihydro-2H-chromen-2-yl)ethanol can be employed as a starting material or a catalyst in asymmetric reactions, leading to the production of chiral drugs with desired stereochemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 1315508-96-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,5,5,0 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1315508-96:
(9*1)+(8*3)+(7*1)+(6*5)+(5*5)+(4*0)+(3*8)+(2*9)+(1*6)=143
143 % 10 = 3
So 1315508-96-3 is a valid CAS Registry Number.

1315508-96-3Upstream product

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