cis-1,3-Dibenzyl-2-imidazolidone-4,5-dicarboxylic Acid

CAS: 51591-75-4

Ref. TR-D422685

Informação sobre produto

• Nome: cis-1,3-Dibenzyl-2-imidazolidone-4,5-dicarboxylic Acid
• Sinónimos: cis-1,3-Dibenzyl-2-oxo-4,5-imidazolidinedicarboxylic Acid, cis-2-oxo-1,3-Bis(phenylmethyl)-4,5-Imidazolidinedicarboxylic Acid, (4R,5S)-rel-2-Oxo-1,3-Bis(phenylmethyl)-4,5-imidazolidinedicarboxylic Acid, (4R,5S)-1,3-dibenzyl-2-oxoimidazolidine-4,5-dicarboxylic acid, (4R,5S)-rel-2-Oxo-1,3-bis(phenylmethyl)-4,5-imidazolidinedicarboxylic acid, 1,3-Dibenzyl-2-Oxoimidazolidine-4,5-Dicarboxylic Acid, 4,5-Imidazolidinedicarboxylic acid, 1,3-dibenzyl-2-oxo-, cis-, 4,5-Imidazolidinedicarboxylic acid, 2-oxo-1,3-bis(phenylmethyl)-, (4R,5S)-rel-, 4,5-Imidazolidinedicarboxylic acid, 2-oxo-1,3-bis(phenylmethyl)-, cis-, cis-1,3-Dibenzyl-2-imidazolidone-4,5-dicarboxylic acid, rel-(4R,5S)-2-Oxo-1,3-bis(phenylmethyl)-4,5-imidazolidinedicarboxylic acid
• CAS: 51591-75-4

Descrição

Applications cis-1,3-Dibenzyl-2-imidazolidone-4,5-dicarboxylic Acid is a reagent in the total synthesis of Biotin. (B389040), growth factor present in minute amounts in every living cell. Plays an indispensable role in numerous naturally occurring carboxylation reactions. Occurs mainly bound to proteins or polypeptides. The richest sources are liver, kidney, pancreas, yeast, and milk. The biotin content of cancerous tumors is higher than that of normal tissue.
References Chen, X. et al.: Chem. Pharm. Bull., 59, 488 (2011); du Vigneaud, et al.: J. Biol. Chem., 146, 475 (1942), Traub, et al.: Nature, 178, 649 (1956), Siegel, H., et al.: Experienta, 37, 789 (1981), Vesely, D.L., Science, 216, 1329 (1982), Hugues, M., et al.: Biochemistry, 31, 12 (1992),

• Marca: TRC

Propriedades químicas

• Peso molecular: 354.36
• Fórmula: C₁₉H₁₈N₂O₅
• Cor/forma: Neat
• InChI: InChI=1S/C19H18N2O5/c22-17(23)15-16(18(24)25)21(12-14-9-5-2-6-10-14)19(26)20(15)11-13-7-3-1-4-8-13/h1-10,15-16H,11-12H2,(H,22,23)(H,24,25)/t15-,16+
• Chave InChI: InChIKey=QSMUFXXTSUEZJA-IYBDPMFKSA-N
• SMILES: O=C(O)[C@@H]1[C@H](C(=O)O)N(Cc2ccccc2)C(=O)N1Cc1ccccc1