(-)-Dibenzyl D-tartrate

CAS Number: 4136-22-5

Molecular Formula: C18H18O6

About (-)-Dibenzyl D-tartrate

(-)-Dibenzyl D-tartrate CAS 4136-22-5 is increasingly sought after by a leading bulk chemical supplier to serve as a high-value chiral building block in the pharmaceutical industry with 98% purity for the synthesis of complex intermediates like chicoric acid and aziridine-2,3-dicarboxylic acid derivatives. Benzyl D-tar...

(-)-Dibenzyl D-tartrate Specifications

CAS Number

4136-22-5

Molecular Formula

C18H18O6

Molecular Weight

330.33 g/mol

IUPAC Name

dibenzyl (2S,3S)-2,3-dihydroxybutanedioate

Canonical SMILES

O[C@@H]([C@H]\(O\)C\(=O\)OCc1ccccc1)C(=O)OCc2ccccc2

InChI Key

LCKIPSGLXMCAOF-HOTGVXAUSA-N

CAS Number

4136-22-5

Molecular Formula

C18H18O6

Molecular Weight

330.33 g/mol

IUPAC Name

dibenzyl (2S,3S)-2,3-dihydroxybutanedioate

Canonical SMILES

O[C@@H]([C@H]\(O\)C\(=O\)OCc1ccccc1)C(=O)OCc2ccccc2

InChI Key

LCKIPSGLXMCAOF-HOTGVXAUSA-N

Molecular Weight

330.33 g/mol

Organic Synthesis Reactant

A versatile chiral reactant employed in the synthesis of complex molecules such as 2,3-bis(8-methoxyoctanoyl) dibenzyl tartrate (DBT) and diesters of aziridine-2,3-dicarboxylic acid derivatives

Pharmaceutical Intermediate

A critical building block used to synthesize (-)-chicoric acid, a potent inhibitor and immunostimulator derived from Echinacea with potential applications in HIV-1 research

Chiral Building Block

An optically active ester utilized as a non-heterocyclic building block in asymmetric synthesis for the development of enantiopure compounds

Academic Research Reagent

A specialized chemical reagent used in laboratories for exploring novel organic reactions, including the preparation of chiral catalysts and ligands for advanced chemical research.