50730-98-8 Usage
Uses
Used in Pharmaceutical Industry:
(2R,3S)-2-Amino-hexane-1,3-diol serves as a chiral building block in the synthesis of various pharmaceuticals. Its unique stereochemistry allows for the creation of enantiomerically pure compounds, which is crucial for ensuring the desired biological activity and minimizing potential side effects.
Used in Asymmetric Catalysis:
In the field of catalysis, (2R,3S)-2-Amino-hexane-1,3-diol acts as a chiral ligand, facilitating asymmetric reactions that produce enantiomerically enriched products. This is particularly important in the synthesis of chiral molecules, such as pharmaceuticals and agrochemicals, where the stereochemistry of the molecule can significantly impact its effectiveness and safety.
Used in Chiral Reagents:
(2R,3S)-2-Amino-hexane-1,3-diol can also be employed as a chiral reagent in various chemical reactions, helping to transfer chirality to other molecules and promoting the formation of specific enantiomers. This is particularly useful in the synthesis of complex organic molecules with multiple chiral centers.
Overall, (2R,3S)-2-Amino-hexane-1,3-diol is a versatile compound with applications in the pharmaceutical, chemical, and catalysis industries, primarily due to its unique stereochemistry and ability to act as a chiral building block, ligand, or reagent.
Check Digit Verification of cas no
The CAS Registry Mumber 50730-98-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,7,3 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 50730-98:
(7*5)+(6*0)+(5*7)+(4*3)+(3*0)+(2*9)+(1*8)=108
108 % 10 = 8
So 50730-98-8 is a valid CAS Registry Number.
50730-98-8Relevant academic research and scientific papers
Amino Acids and Peptides; 70. Optically Active α-Amino Acids, N-Boc-Aminoaldehydes and α-Amino-β-hydroxy Acids from 2,3-Epoxy Alcohols
Schmidt, Ulrich,Respondek, Mathias,Lieberknecht, Albrecht,Werner, Juergen,Fischer, Peter
, p. 256 - 261 (2007/10/02)
Trichloroacetimidic esters of 2,3-epoxy alcohols are transformed into oxazolines 5 and dihydrooxazines 6, respectively, depending on the structure of the educts and the catalyst.The five-membered ring compounds 5 are transformed into erythro-α-amino-β-hydroxy acids (60-70percent from epoxy alcohols) via axazolidinones 11, 12, and 13. α-Amino acids and α-substituted α-amino acids 10 as well as the corresponding aldehydes 9 are obtained from the dihydrooxazines 6 (50-60percent from epoxy alcohols).
