CAS 13638-89-6: diethyl (2R,3S)-2,3-diphenylbutanedioate

Description: Diethyl (2R,3S)-2,3-diphenylbutanedioate, with CAS number 13638-89-6, is an organic compound characterized by its ester functional groups and a chiral center, which contributes to its stereochemistry. This compound features two ethyl ester groups attached to a butanedioic acid backbone, specifically at the 2 and 3 positions, each substituted with phenyl groups. The presence of these phenyl groups enhances its hydrophobic character and may influence its solubility in organic solvents. The stereochemistry (2R,3S) indicates that the compound exists in a specific spatial arrangement, which can affect its reactivity and interactions with biological systems. Typically, compounds like this may be used in synthetic organic chemistry, potentially serving as intermediates in the synthesis of more complex molecules or as chiral building blocks. Its properties, such as melting point, boiling point, and reactivity, would depend on the specific conditions and the presence of other functional groups in a reaction environment.

Formula: C₂₀H₂₂O₄

InChI: InChI=1/C20H22O4/c1-3-23-19(21)17(15-11-7-5-8-12-15)18(20(22)24-4-2)16-13-9-6-10-14-16/h5-14,17-18H,3-4H2,1-2H3/t17-,18+

Synonyms:

• Butanedioic acid, 2,3-diphenyl-, diethyl ester, (2R,3S)-
• Diethyl (2R,3S)-2,3-diphenylsuccinate

1,4-Diethyl (2S,3R)-2,3-diphenylbutanedioate

CAS: 13638-89-6

• Molecular weight: 326.38628g/mol

Meso-2,3-Diphenyl-succinic acid diethyl ester

CAS: 13638-89-6

• Purity: 98.0%
• Color and Shape: Solid
• Molecular weight: 326.392

Meso-2,3-diphenyl-succinic acid diethyl ester

CAS: 13638-89-6

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• Formula: C₂₀H₂₂O₄
• Purity: Min. 95%
• Molecular weight: 326.4 g/mol