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Home  > (2R,3R)-2,3-dihydroxybutanedioic acid; 5-bromo-N-(4,5-dihydro-1H-imidazol-2-yl)quinoxalin-6-amine

AC92298

70359-46-5 | (2R,3R)-2,3-dihydroxybutanedioic acid; 5-bromo-N-(4,5-dihydro-1H-imidazol-2-yl)quinoxalin-6-amine

Packsize Purity Availability Price Discounted Price    Quantity
100mg 98% in stock $35.00 $24.00 -   +
250mg 98% in stock $43.00 $30.00 -   +
1g 98% in stock $65.00 $45.00 -   +
5g 98% in stock $189.00 $132.00 -   +
25g 98% in stock $755.00 $528.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AC92298
Chemical Name: (2R,3R)-2,3-dihydroxybutanedioic acid; 5-bromo-N-(4,5-dihydro-1H-imidazol-2-yl)quinoxalin-6-amine
CAS Number: 70359-46-5
Molecular Formula: C15H16BrN5O6
Molecular Weight: 442.2214
MDL Number: MFCD07773072
SMILES: O[C@H]([C@H](C(=O)O)O)C(=O)O.Brc1c(ccc2c1nccn2)NC1=NCCN1

 

Computed Properties
Complexity: 442  
Covalently-Bonded Unit Count: 2  
Defined Atom Stereocenter Count: 2  
Heavy Atom Count: 27  
Hydrogen Bond Acceptor Count: 9  
Hydrogen Bond Donor Count: 6  
Rotatable Bond Count: 5  

 

 

Upstream Synthesis Route
  • 6-Quinoxalinamine, 5-bromo-N-(4,5-dihydro-1H-imidazol-2-yl)-, (2R,3R)-2,3-dihydroxybutanedioate (1:1) is a versatile compound commonly utilized in chemical synthesis processes. Its unique structure and properties make it a valuable reagent in various chemical reactions. This compound is frequently employed as a key intermediate in the synthesis of pharmaceutical compounds, agrochemicals, and specialty chemicals. Its ability to undergo selective transformations and functional group interconversions makes it a valuable tool for organic chemists seeking to access complex molecular structures. In addition, its stereochemical arrangement provides opportunities for chiral induction in asymmetric synthesis strategies. Overall, 6-Quinoxalinamine, 5-bromo-N-(4,5-dihydro-1H-imidazol-2-yl)-, (2R,3R)-2,3-dihydroxybutanedioate (1:1) plays a crucial role in advancing the field of chemical synthesis by enabling the efficient construction of diverse and intricate chemical entities.
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