(S)-2-(2-hydroxy-3-(4-(3-oxomorpholino)phenylamino)propyl)isoindoline-1,3-dione - Names and Identifiers
Name | 2-[(2R)-2-hydroxy-3-{[4-(3-oxomorpholin-4-yl)phenyl]amino}propyl]-1H-isoindole-1,3(2H)-dione
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Synonyms | (S)-2-(2-hydroxy-3-(4-(3-oxomorpholino)phenylamino)propyl)isoindoline-1,3-dione 1H-Isoindole-1,3(2H)-dione,2-[(2R)-2-hydroxy-3-[[4-(3-oxo-4-morpholinyl)phenyl]amino]propyl 2-[(2R)-2-Hydroxy-3-[[4-(3-oxo-4-morpholinyl)phenyl]amino]propyl]-1H-isoindole-1,3(2H)-dione 2-[(2R)-2-hydroxy-3-{[4-(3-oxomorpholin-4-yl)phenyl]amino}propyl]-1H-isoindole-1,3(2H)-dione 1H-ISOINDOLE-1,3(2H)-DIONE, 2-[(2R)-2-HYDROXY-3-[[4-(3-OXO-4-MORPHOLINYL)PHENYL]AMINO]PROPYL]- 1H-Isoindole-1,3(2H)-dione, 2-[(2R)-2-hydroxy-3-[[4-(3-oxo-4-morpholinyl)phenyl]amino]propyl]-
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CAS | 446292-07-5
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EINECS | 610-200-5 |
InChI | InChI=1/C21H21N3O5/c25-16(12-24-20(27)17-3-1-2-4-18(17)21(24)28)11-22-14-5-7-15(8-6-14)23-9-10-29-13-19(23)26/h1-8,16,22,25H,9-13H2/t16-/m1/s1 |
(S)-2-(2-hydroxy-3-(4-(3-oxomorpholino)phenylamino)propyl)isoindoline-1,3-dione - Physico-chemical Properties
Molecular Formula | C21H21N3O5
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Molar Mass | 395.41 |
Density | 1.421g/cm3 |
Boling Point | 734.905°C at 760 mmHg |
Flash Point | 398.256°C |
Vapor Presure | 0mmHg at 25°C |
pKa | 13.91±0.20(Predicted) |
Storage Condition | under inert gas (nitrogen or Argon) at 2–8 °C |
Refractive Index | 1.672 |
Use | This product is for scientific research only and shall not be used for other purposes. |
(S)-2-(2-hydroxy-3-(4-(3-oxomorpholino)phenylamino)propyl)isoindoline-1,3-dione - Upstream Downstream Industry
(S)-2-(2-hydroxy-3-(4-(3-oxomorpholino)phenylamino)propyl)isoindoline-1,3-dione - Introduction
2-[(2R)-2-hydroxy-3-{[4-(3-oxomorpholin-4-yl)phenyl]amino}propyl]-1H-isoindole-1,3(2H)-dione is an organic compound with the following properties:
Physical Properties:
-Appearance: White crystalline solid
-Molecular weight: 446.52g/mol
-melting point: about 220-225 ℃
Chemical Properties:
-It is a ketone compound containing hydroxyl and amino functional groups. Its structure includes an isoindole nucleus and a benzene ring.
-Under acidic conditions, it can lose the hydrogen ion in the hydroxyl group and form a carbanion.
-It can react with other compounds for condensation, acylation and substitution.
Use:
-It can be used as an intermediate for the synthesis of organic compounds and for the preparation of other drugs, dyes and functional materials.
-It has biological activities such as anti-tumor, anti-inflammatory and antioxidant, so it has potential application value in the field of drug research.
Preparation Method:
-It can be prepared by chemical synthesis, generally by reacting appropriate raw materials under appropriate reaction conditions to obtain the target product.
Safety Information:
-Its specific safety information requires reference to the relevant Chemical Safety Data Sheet (MSDS).
-During handling and use, observe appropriate laboratory safety procedures, wear appropriate protective equipment, and avoid contact with skin, eyes, and respiratory tract.
Last Update:2024-04-09 02:00:46