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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

4,7-Epoxy-1H-isoindole-1,3(2H)-dione, 3a,4,7,7a-tetrahydro-2-hydroxy-

ON1C(=O)C2C(C1=O)C1OC2C=C1 Request for Quotation
Chemical Name: 4,7-Epoxy-1H-isoindole-1,3(2H)-dione, 3a,4,7,7a-tetrahydro-2-hydroxy-
CAS Number: 5596-17-8
Product Number: AG0033C8(AGN-PC-004B04)
Synonyms:
MDL No:
Molecular Formula: C8H7NO4
Molecular Weight: 181.1455

Identification/Properties

Properties
MP:
194 °C (dec.);(lit.);
BP:
384.8°C at 760 mmHg
Storage:
Inert atmosphere;-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
181.147g/mol
XLogP3:
-1.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
181.038g/mol
Monoisotopic Mass:
181.038g/mol
Topological Polar Surface Area:
66.8A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
307
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
4
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-Hydroxy-3,6-epoxy-1,2,3,6-tetrahydrophthalimide, also known as $name$, serves as a versatile reagent in chemical synthesis. Its unique structure and reactivity make it valuable in a variety of organic transformations.$name$ plays a crucial role in ring-opening reactions, particularly in the formation of epoxide derivatives. This compound can act as a potent electrophile, participating in nucleophilic additions to introduce various functional groups onto the epoxy ring. Additionally, $name$ can undergo rearrangement reactions, leading to the generation of diverse molecular scaffolds.Furthermore, $name$ is utilized in the synthesis of heterocyclic compounds, where its oxirane moiety enables the construction of complex ring systems with high regio- and stereo-selectivity. Its ability to facilitate the formation of carbon-carbon and carbon-heteroatom bonds makes it a valuable tool for the creation of pharmaceutical intermediates and natural product analogs.In summary, the application of N-Hydroxy-3,6-epoxy-1,2,3,6-tetrahydrophthalimide in chemical synthesis extends to its role as a versatile building block for the construction of diverse molecular architectures with synthetic utility and potential biological activity.