1H-Isoindole-1,3(2H)-dione, 4,5,6,7-tetrahydro-


Chemical Name: 1H-Isoindole-1,3(2H)-dione, 4,5,6,7-tetrahydro-
CAS Number: 4720-86-9
Product Number: AG00I8MC(AGN-PC-0JKNI7)
Synonyms:
MDL No:
Molecular Formula: C8H9NO2
Molecular Weight: 151.1626

Identification/Properties


Properties
MP:
168℃-172℃
BP:
324.3°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid

Safety Information


GHS Pictogram:
Signal Word:
Danger
UN#:
2811
Hazard Statements:
H301-H311-H331-H341
Precautionary Statements:
P201-P202-P261-P264-P270-P271-P280-P302+P352-P304+P340-P308+P313-P310-P330-P361-P403+P233-P405-P501
Class:
6.1
Packing Group:

NMR Spectrum


Other Analytical Data


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Chemical Structure



4,5,6,7-Tetrahydro-1H-isoindole-1,3(2H)-dione, commonly referred to in chemical synthesis as $name$, serves as a versatile building block for creating complex organic molecules. This compound is widely utilized in the development of pharmaceuticals, agrochemicals, and materials due to its unique structural properties and reactivity.In chemical synthesis, $name$ can act as a key intermediate in the production of various biologically active compounds. Its cyclic structure provides a rigid framework for establishing stereochemical control during reactions, making it a valuable tool for designing chiral molecules with specific biological effects.Furthermore, the carbonyl groups present in $name$ enable it to participate in a range of chemical transformations, such as nucleophilic addition and oxidation reactions. By strategically incorporating this compound into synthetic pathways, chemists can efficiently access a diverse array of molecular architectures with a high degree of control over regioselectivity and stereochemistry.Overall, the strategic use of 4,5,6,7-Tetrahydro-1H-isoindole-1,3(2H)-dione in chemical synthesis enables the synthesis of complex molecules with potential applications in various industries, highlighting its importance as a versatile building block in organic chemistry.