1009282-06-7 Usage
Description
1-(2,3,5,6-TetraMethylphenylsulfonyl)-L-proline, 96% is a high purity chemical compound that is a derivative of sulfonyl proline. It is widely utilized in organic synthesis and pharmaceutical research due to its ability to act as a chiral auxiliary in asymmetric synthesis, controlling the stereochemistry of reactions. 1-(2,3,5,6-TetraMethylphenylsulfonyl)-L-proline, 96% is also employed as a building block for the synthesis of various pharmaceutical compounds and fine chemicals, making it a valuable asset in research and industrial applications that demand precision and reliability.
Uses
Used in Pharmaceutical Research:
1-(2,3,5,6-TetraMethylphenylsulfonyl)-L-proline, 96% is used as a chiral auxiliary for controlling the stereochemistry of reactions in pharmaceutical research. Its ability to influence the spatial arrangement of molecules during synthesis is crucial for the development of new drugs with desired properties and reduced side effects.
Used in Organic Synthesis:
In the field of organic synthesis, 1-(2,3,5,6-TetraMethylphenylsulfonyl)-L-proline, 96% is used as a building block for the synthesis of various pharmaceutical compounds and fine chemicals. Its high purity level ensures that the synthesized products are of excellent quality, making it a preferred choice for researchers and chemists.
Used in Asymmetric Synthesis:
1-(2,3,5,6-TetraMethylphenylsulfonyl)-L-proline, 96% is used as a chiral auxiliary in asymmetric synthesis, a technique that allows for the creation of molecules with specific three-dimensional structures. This is particularly important in the development of enantiomerically pure compounds, which can have different biological activities and are often required for pharmaceutical applications.
Used in Research and Industrial Applications:
Due to its high purity level, 1-(2,3,5,6-TetraMethylphenylsulfonyl)-L-proline, 96% is suitable for use in research and industrial applications where precise and reliable results are required. Its versatility in controlling stereochemistry and its role as a building block make it a valuable tool for scientists and researchers in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 1009282-06-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,9,2,8 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1009282-06:
(9*1)+(8*0)+(7*0)+(6*9)+(5*2)+(4*8)+(3*2)+(2*0)+(1*6)=117
117 % 10 = 7
So 1009282-06-7 is a valid CAS Registry Number.
