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Thermo Scientific Chemicals
(2S,3aS,7aS)-Octahydroindole-2-carboxylic acid, 98%
CAS: 80875-98-5 | C9H15NO2 | 169.224 g/mol
化学物質識別子
CAS80875-98-5
IUPAC Nameoctahydro-1H-indole-2-carboxylic acid
Molecular FormulaC9H15NO2
InChI KeyCQYBNXGHMBNGCG-UHFFFAOYNA-N
SMILESOC(=O)C1CC2CCCCC2N1
さらに表示
仕様
スペックシート
スペックシートFormPowder
Appearance (Color)White
Assay (Aqueous acid-base Titration)≥97.5 to ≤102.5%
Optical Rotation-50.0 ± 1.0? (C=1 in methanol)
An intermediate in the synthesis of Perindopril. The completely diastereoselective α-alkylation of oxazolidinone provides a very convenient and concise route to enantiopure α-tetrasubstituted derivatives of this Oic stereoisomer.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
An intermediate in the synthesis of Perindopril. The completely diastereoselective α-alkylation of oxazolidinone provides a very convenient and concise route to enantiopure α-tetrasubstituted derivatives of this Oic stereoisomer.
Solubility
Soluble in methanol and water.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents. Store at -20°C.
An intermediate in the synthesis of Perindopril. The completely diastereoselective α-alkylation of oxazolidinone provides a very convenient and concise route to enantiopure α-tetrasubstituted derivatives of this Oic stereoisomer.
Solubility
Soluble in methanol and water.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents. Store at -20°C.
RUO – Research Use Only
General References:
- Francisco J. Sayago,; M. Isabel Calaza,; Ana I. Jiménez,; Carlos Cativiela. A straightforward route to enantiopure α-substituted derivatives of (2S,3aS,7aS)-octahydroindole-2-carboxylic acid. Journal name. 2009, 65(27) ,5174-5180.
- Francisco J. Sayago,; M. Isabel Calaza,; Ana I. Jiménez,; Carlos Cativiela. Versatile methodology for the synthesis and α-functionalization of (2R,3aS,7aS)-octahydroindole-2-carboxylic acid. Tetrahedron. 2008, 64(1), 84-91.