Determine the necessary mass, volume, or concentration for preparing a solution.
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Product Describtion:
(S)-(-)-Thalidomide is an optically active isomer of Thalidomide. Inhibits FGF-induced angiogenesis and replication of human immunodeficiency virus type 1.
Product Application:
Optically active isomer of Thalidomide, which inhibits FGF-induced angiogenesis. Inhibits replication of human immunodeficiency virus type 1. Teratogenic sedative.
Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Clase | Isoindoles and derivatives |
| Subclass | Isoindolines |
| Intermediate Tree Nodes | Isoindolones |
| Direct Parent | Phthalimides |
| Alternative Parents | Alpha amino acids and derivatives Isoindoles Tetrahydropyridines N-substituted carboxylic acid imides Benzenoids N-acylimines Lactims Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Phthalimide - Alpha-amino acid or derivatives - Isoindole - Tetrahydropyridine - Hydropyridine - Carboxylic acid imide, n-substituted - Benzenoid - Carboxylic acid imide - N-acylimine - Lactim - Azacycle - Carboxylic acid derivative - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Carbonyl group - Aromatic heteropolycyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as phthalimides. These are aromatic heterocyclic compounds containing a 1,3-dioxoisoindoline moiety. They are imide derivatives of phthalic anhydrides. |
| External Descriptors | 2-(2,6-dioxopiperidin-3-yl)-1H-isoindole-1,3(2H)-dione |
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Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
| Certificate of Analysis | Aug 07, 2025 | T340150 | |
| Certificate of Analysis | Aug 07, 2025 | T340150 | |
| Certificate of Analysis | Aug 07, 2025 | T340150 | |
| Certificate of Analysis | Aug 07, 2025 | T340150 | |
| Certificate of Analysis | Aug 07, 2025 | T340150 | |
| Certificate of Analysis | Aug 07, 2025 | T340150 | |
| Certificate of Analysis | Feb 02, 2024 | T340150 | |
| Certificate of Analysis | Feb 02, 2024 | T340150 | |
| Certificate of Analysis | Feb 02, 2024 | T340150 | |
| Certificate of Analysis | Feb 02, 2024 | T340150 | |
| Certificate of Analysis | Jun 12, 2022 | T340150 | |
| Certificate of Analysis | Jun 12, 2022 | T340150 | |
| Certificate of Analysis | Jun 12, 2022 | T340150 | |
| Certificate of Analysis | Jun 12, 2022 | T340150 | |
| Certificate of Analysis | Jun 12, 2022 | T340150 |
| Solubilidad | Sparingly soluble in Water, Methanol, Ethanol, Acetone, Ethyl Acetate and Butyl Acetate |
|---|---|
| Sensibilidad | light sensitive |
| Punto de inflamación (°C) | 262.1°C |
| Punto de fusión (°C) | >251ºC |
| Peso molecular | 258.230 g/mol |
| XLogP3 | 0.300 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 1 |
| Exact Mass | 258.064 Da |
| Monoisotopic Mass | 258.064 Da |
| Topological Polar Surface Area | 83.600 Ų |
| Heavy Atom Count | 19 |
| Formal Charge | 0 |
| Complexity | 449.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |