Benzamide,3,5-dichloro-N-[[(2S)-1-ethyl-2-pyrrolidinyl]methyl]-2-hydroxy-6-methoxy-, (2R,3R)-2,3-dihydroxybutanedioate (1:1) (salt)


Chemical Name: Benzamide,3,5-dichloro-N-[[(2S)-1-ethyl-2-pyrrolidinyl]methyl]-2-hydroxy-6-methoxy-, (2R,3R)-2,3-dihydroxybutanedioate (1:1) (salt)
CAS Number: 98185-20-7
Product Number: AG0036OH(AGN-PC-0W7Y6V)
Synonyms:
MDL No:
Molecular Formula: C19H26Cl2N2O9
Molecular Weight: 497.3237

Identification/Properties


Properties
Form:
Solid
Computed Properties
Molecular Weight:
497.322g/mol
Hydrogen Bond Donor Count:
6
Hydrogen Bond Acceptor Count:
9
Rotatable Bond Count:
7
Exact Mass:
496.102g/mol
Monoisotopic Mass:
496.102g/mol
Topological Polar Surface Area:
181A^2
Heavy Atom Count:
32
Formal Charge:
0
Complexity:
532
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
3
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

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Chemical Structure



The S(-)-Raclopride (+)-tartrate salt is a highly valuable compound used in chemical synthesis for its enantiomeric purity. This specific form of Raclopride offers precise stereochemistry that is crucial for designing and synthesizing chiral molecules in pharmaceutical and chemical research.Due to its enantiomeric composition, the S(-)-Raclopride (+)-tartrate salt serves as a versatile chiral building block in asymmetric synthesis. It enables chemists to create complex molecular structures with defined stereochemistry, which is essential for developing new pharmaceuticals, agrochemicals, and advanced materials.In organic chemistry, this compound plays a key role in enantioselective transformations and catalytic reactions. Its unique stereochemistry allows for the selective formation of specific enantiomers, aiding in the production of optically pure compounds with improved biological activity and reduced side effects.Overall, the application of S(-)-Raclopride (+)-tartrate salt in chemical synthesis offers a powerful tool for researchers and synthetic chemists seeking to access chirally pure compounds and advance their understanding of molecular interactions and chemical reactivity.