CAS 21715-90-2
:3a,4,7,7a-Tetrahydro-2-hydroxy-4,7-methano-1H-isoindole-1,3(2H)-dione
Description:
3a,4,7,7a-Tetrahydro-2-hydroxy-4,7-methano-1H-isoindole-1,3(2H)-dione, with the CAS number 21715-90-2, is a chemical compound that belongs to the class of isoindole derivatives. This substance features a bicyclic structure characterized by a fused isoindole ring system, which contributes to its unique chemical properties. The presence of a hydroxyl group (-OH) indicates potential for hydrogen bonding, influencing its solubility and reactivity. The compound is likely to exhibit moderate polarity due to the functional groups present. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as isoindole derivatives are often explored for their biological activities. Additionally, the compound may participate in various chemical reactions, including nucleophilic substitutions and cycloadditions, making it of interest for synthetic organic chemistry. Overall, the characteristics of this compound highlight its significance in both theoretical studies and practical applications within the field of chemistry.
Formula:C9H9NO3
InChI:InChI=1S/C9H9NO3/c11-8-6-4-1-2-5(3-4)7(6)9(12)10(8)13/h1-2,4-7,13H,3H2
InChI key:InChIKey=ZUSSTQCWRDLYJA-UHFFFAOYSA-N
SMILES:O=C1C2C(C3CC2C=C3)C(=O)N1O
Synonyms:- (3aR,4S,7R,7aS)-2-hydroxy-3a,4,7,7a-tetrahydro-1H-4,7-methanoisoindole-1,3(2H)-dione
- (3aR,4S,7S,7aR)-2-hydroxy-3a,4,7,7a-tetrahydro-1H-4,7-methanoisoindole-1,3(2H)-dione
- 2-hydroxy-3a,4,7,7a-tetrahydro-1H-4,7-methanoisoindole-1,3(2H)-dione
- 3,5-Dioxo-4-azatricyclo[5.2.1.0<sup>2</sup>′<sup>6</sup>]dec-8-en-4-ol
- 3a,4,7,7a-Tetrahydro-2-hydroxy-4,7-methano-1H-isoindole-1,3(2H)-dione
- 4,7-Methano-1H-isoindole-1,3(2H)-dione, 3a,4,7,7a-tetrahydro-2-hydroxy-
- 5-Norbornene-2,3-dicarboximide, N-hydroxy-
- Honb
- N-Hydroxy-5-bicyclo[2.2.1]heptene-2,3-dicarboximide
- N-Hydroxy-5-norbornene-endo-2,3-dicarboximide
- N-Hydroxybicyclo[2.2.1]hept-5-ene-2,3-dicarboximide
- N-hydroxy-5-norbornene-2.3-dicarboxylimide
- NSC 100740
- NSC 12953
- endo-N-Hydroxy-5-norbornene-2,3-dicarboximide
- See more synonyms
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Found 7 products.
N-Hydroxy-5-norbornene-2,3-dicarboximide [for Peptide Synthesis]
CAS:Formula:C9H9NO3Purity:>99.0%(T)Color and Shape:White to Almost white powder to crystalMolecular weight:179.18endo-N-Hydroxy-5-norbornene-2,3-dicarboximide, 97%
CAS:<p>It decreases racemization in peptide synthesis and inhibits formation of N-acylureas. 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</p>Formula:C9H9NO3Purity:97%Color and Shape:Crystals or powder or crystalline powder or fused solid, White to pale creamMolecular weight:179.182-Hydroxy-3a,4,7,7a-tetrahydro-1H-4,7-methanoisoindole-1,3(2H)-dione
CAS:Formula:C9H9NO3Purity:98%Color and Shape:SolidMolecular weight:179.1727endo-N-Hydroxybicyclo[2.2.1]hept-5-ene-2,3-dicarboximide
CAS:<p>endo-N-Hydroxybicyclo[2.2.1]hept-5-ene-2,3-dicarboximide</p>Purity:98%Color and Shape:Beige SolidMolecular weight:179.17g/molN-Hydroxy-5-norbornene-2,3-dicarboximide
CAS:Formula:C9H9NO3Purity:95.0%Color and Shape:Solid, Powder or Crystalline Powder or Solid or ChunksMolecular weight:179.058HONB
CAS:Controlled Product<p>Applications HONB is used in solution-phase peptide synthesis. Used in the synthesis of enkephalin analogs.<br>References Mahindra, A. et al.: Tetrahedron Lett., 53, 6391 (2012); Irina, B. et al.: Eur. J. Med. Chem., 33, 255 (1998);<br></p>Formula:C9H9NO3Color and Shape:NeatMolecular weight:179.17






