9H-Carbazole, 9-(oxiranylmethyl)-|52131-82-5,AngeneChemical

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9H-Carbazole, 9-(oxiranylmethyl)-

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Chemical Name:	9H-Carbazole, 9-(oxiranylmethyl)-
CAS Number:	52131-82-5
Product Number:	AG00D9N2(AGN-PC-0JVOCQ)
Synonyms:
MDL No:
Molecular Formula:	C15H13NO
Molecular Weight:	223.2698

Identification/Properties
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NMR Spectrum
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Identification/Properties

Properties

MP:

110℃

Form:

Solid

Computed Properties

Molecular Weight:

223.275g/mol

XLogP3:

Hydrogen Bond Donor Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

Exact Mass:

223.1g/mol

Monoisotopic Mass:

223.1g/mol

Topological Polar Surface Area:

17.5A^2

Heavy Atom Count:

Formal Charge:

Complexity:

271

Isotope Atom Count:

Defined Atom Stereocenter Count:

Undefined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Undefined Bond Stereocenter Count:

Covalently-Bonded Unit Count:

Compound Is Canonicalized:

Yes

Safety Information

GHS Pictogram:

N/A

Signal Word:

UN#:

Hazard Statements:

Precautionary Statements:

Class:

Packing Group:

NMR Spectrum

Other Analytical Data

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Chemical Structure

9-(Oxiran-2-ylmethyl)-9H-carbazole, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound is particularly valued for its role as a key intermediate in the production of various organic compounds. Its unique structure containing both an oxirane ring and a carbazole moiety makes it a valuable building block in the synthesis of complex molecules.In chemical synthesis, $name$ serves as a powerful tool for introducing functional groups or modifying existing structures. The oxirane group in $name$ is highly reactive and can undergo a variety of transformations, such as ring-opening reactions, enabling the attachment of different substituents. This flexibility allows chemists to tailor the properties of the final compound for specific applications.Additionally, the carbazole portion of $name$ plays an essential role in the synthesis of heterocyclic compounds and organic materials. Carbazole derivatives have shown promising properties in various fields, including organic electronics, materials science, and pharmaceuticals. By incorporating the carbazole unit from $name$ into target molecules, researchers can access compounds with enhanced functionalities and desirable characteristics.Overall, the strategic placement of the oxirane and carbazole functionalities in 9-(Oxiran-2-ylmethyl)-9H-carbazole makes it a valuable intermediate for designing and synthesizing a wide range of organic compounds with diverse applications.