Carbamic acid,[(1S,2R)-2-hydroxy-3-[(2-methylpropyl)[(4-nitrophenyl)sulfonyl]amino]-1-(phenylmethyl)propyl]-, (3S)-tetrahydro-3-furanyl ester


Chemical Name: Carbamic acid,[(1S,2R)-2-hydroxy-3-[(2-methylpropyl)[(4-nitrophenyl)sulfonyl]amino]-1-(phenylmethyl)propyl]-, (3S)-tetrahydro-3-furanyl ester
CAS Number: 160231-69-6
Product Number: AG001RRL(AGN-PC-0Q7UY2)
Synonyms:
MDL No:
Molecular Formula: C25H33N3O8S
Molecular Weight: 535.6098

Identification/Properties


Computed Properties
Molecular Weight:
535.612g/mol
XLogP3:
3.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
9
Rotatable Bond Count:
12
Exact Mass:
535.199g/mol
Monoisotopic Mass:
535.199g/mol
Topological Polar Surface Area:
159A^2
Heavy Atom Count:
37
Formal Charge:
0
Complexity:
830
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:
1
Compound Is Canonicalized:
Yes

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Chemical Structure



(S)-Tetrahydrofuran-3-yl ((2S,3R)-3-hydroxy-4-(N-isobutyl-4-nitrophenylsulfonamido)-1-phenylbutan-2-yl)carbamate is a versatile compound used in chemical synthesis for its ability to participate in various reactions to create complex molecules. Its unique structure allows it to serve as a key building block in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. This compound is particularly valued for its stereochemical properties, which enable precise control over the configuration of newly formed bonds during synthetic processes. By incorporating (S)-Tetrahydrofuran-3-yl ((2S,3R)-3-hydroxy-4-(N-isobutyl-4-nitrophenylsulfonamido)-1-phenylbutan-2-yl)carbamate into synthetic pathways, chemists can efficiently construct intricate molecular structures with high levels of stereochemical purity.