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Absolute stereochemistry is the precise three-dimensional arrangement of atoms in a molecule, particularly focusing on the orientation of chiral centers. Chirality is a property of molecules that are non-superimposable on their mirror images, and it is defined by the absolute configuration of these molecules. This concept is crucial for determining the physical, chemical, and biological properties of substances, as well as their efficacy and potential side effects in pharmaceuticals. Mastery of absolute stereochemistry is essential in organic chemistry and drug development.
Usage:
Used in Pharmaceutical Development:
Absolute stereochemistry is used as a critical factor in the development of pharmaceuticals, as it influences the efficacy and potential side effects of a drug. The specific spatial arrangement of chiral centers can greatly impact how a drug interacts with its target, leading to differences in potency, selectivity, and safety.
Used in Organic Chemistry:
In the field of organic chemistry, absolute stereochemistry is used as a fundamental concept for understanding the structure and reactivity of molecules. It helps chemists predict and control the outcomes of chemical reactions, particularly those involving chiral compounds, ensuring the desired products are synthesized with the correct stereochemistry.
Used in Quality Control and Analysis:
Absolute stereochemistry is utilized in quality control and analysis to ensure that pharmaceutical products have the correct stereochemistry, which is essential for their intended biological activity. Analytical techniques such as X-ray crystallography, nuclear magnetic resonance (NMR) spectroscopy, and circular dichroism (CD) are employed to determine and confirm the absolute stereochemistry of molecules in drug substances and formulations.
Used in Drug Design:
In drug design, absolute stereochemistry is used as a guiding principle to create new molecules with specific biological activities. By understanding the relationship between stereochemistry and biological function, researchers can design drugs that are more effective and have fewer side effects, leading to improved therapeutic outcomes for patients.

883697-32-3

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883697-32-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 883697-32-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,3,6,9 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 883697-32:
(8*8)+(7*8)+(6*3)+(5*6)+(4*9)+(3*7)+(2*3)+(1*2)=233
233 % 10 = 3
So 883697-32-3 is a valid CAS Registry Number.

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