939983-16-1 Usage
Uses
Used in Organic Synthesis:
(2R,3S)-Rel-2,3-bis(4-chlorophenyl)-2,3-butanediamine is used as a building block in organic synthesis for the creation of various complex organic molecules. Its unique structure and functional groups allow for versatile chemical reactions, enabling the synthesis of a wide range of compounds with potential applications in different industries.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (2R,3S)-Rel-2,3-bis(4-chlorophenyl)-2,3-butanediamine is utilized as a starting material or intermediate in the development of new drugs. Its chiral nature and potential biological activity make it a promising candidate for the synthesis of enantiomerically pure pharmaceutical compounds, which can exhibit improved efficacy and reduced side effects compared to their racemic counterparts.
Used in Chiral Catalysts:
(2R,3S)-Rel-2,3-bis(4-chlorophenyl)-2,3-butanediamine can be employed as a chiral catalyst in asymmetric synthesis, a technique used to produce enantiomerically pure compounds. Its unique stereochemistry allows for selective activation of substrates, leading to the formation of desired enantiomers with high selectivity and yield.
Used in Analytical Chemistry:
In analytical chemistry, (2R,3S)-Rel-2,3-bis(4-chlorophenyl)-2,3-butanediamine can be used as a chiral derivatizing agent for the resolution and analysis of enantiomers. Its ability to selectively react with specific enantiomers can help in the separation and detection of chiral compounds, providing valuable information about their absolute configuration and stereochemistry.
Used in Materials Science:
(2R,3S)-Rel-2,3-bis(4-chlorophenyl)-2,3-butanediamine can be incorporated into the design and synthesis of chiral materials with unique properties, such as optical activity, self-assembly behavior, and specific interactions with other chiral molecules. These materials can find applications in various fields, including sensors, drug delivery systems, and chiral separation techniques.
Check Digit Verification of cas no
The CAS Registry Mumber 939983-16-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,9,9,8 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 939983-16:
(8*9)+(7*3)+(6*9)+(5*9)+(4*8)+(3*3)+(2*1)+(1*6)=241
241 % 10 = 1
So 939983-16-1 is a valid CAS Registry Number.
939983-16-1Relevant academic research and scientific papers
4,4,5,5, Tetrasubstituted imidazolines
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Page/Page column 12/2, (2008/06/13)
There is provided a compound of formula I and the pharmaceutically acceptable salts and esters thereof wherein X1, X2, R1, R2, R3, R4, R5 and R6 are herein described. The compounds exhibit activity as anticancer agents.
