95352

(−)-Dibenzyl D-tartrate

≥98.0% (sum of enantiomers, HPLC)

• Fórmula empírica (Notação de Hill): C₁₈H₁₈O₆
• Número CAS: 4136-22-5
• Peso molecular: 330.33
• Beilstein: 4787873
• Número MDL: MFCD01863133
• Código UNSPSC: 12352108
• ID de substância PubChem: 57653674
• NACRES: NA.22

Propriedades

• Nível de qualidade: 100
• Ensaio: ≥98.0% (sum of enantiomers, HPLC)
• Formulário: powder
• atividade óptica: [α]20/D −12.5±1°, c = 1.1% in acetone
• pf: 66-70 °C
• grupo funcional: ester; hydroxyl; phenyl
• cadeia de caracteres SMILES: O[C@@H]([C@H](O)C(=O)OCc1ccccc1)C(=O)OCc2ccccc2
• InChI: 1S/C18H18O6/c19-15(17(21)23-11-13-7-3-1-4-8-13)16(20)18(22)24-12-14-9-5-2-6-10-14/h1-10,15-16,19-20H,11-12H2/t15-,16-/m0/s1
• chave InChI: LCKIPSGLXMCAOF-HOTGVXAUSA-N

Descrição

Aplicação

(-)-Dibenzyl D-tartrate can be employed as a reactant to synthesize:

• 2,3-bis(8-Methoxyoctanoyl) dibenzyl tartrate (DBT) by reacting with 8-methoxyoctanoic acid in the presence of 1-ethyl-3-(3-(dimethylamino)propyl)carbodiimide (EDCI) as a coupling reagent.[1]
• (-)-Chicoric acid (2,3-bis{[3-(3,4-dihydroxyphenyl)-1-oxoprop-2-enyl]oxy}butanedioic acid), as a potent inhibitor.[2]
• Diesters of aziridine-2,3-dicarboxylic acid derivatives.[3]

Informações de segurança

• Código de classe de armazenamento: 11 - Combustible Solids
• Classe de risco de água (WGK): WGK 3
• Ponto de fulgor (°F): Not applicable
• Ponto de fulgor (°C): Not applicable
• Equipamento de proteção individual: Eyeshields, Gloves, type N95 (US)