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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)-

9H-Carbazole, 4-[(2S)-oxiranylmethoxy]-

c1cc(OC[C@@H]2CO2)c2c(c1)[nH]c1c2cccc1 Request for Quotation
Chemical Name: 9H-Carbazole, 4-[(2S)-oxiranylmethoxy]-
CAS Number: 95093-95-1
Product Number: AG005TF3(AGN-PC-0OO18H)
Synonyms:
MDL No:
Molecular Formula: C15H13NO2
Molecular Weight: 239.2692

Identification/Properties

Properties
MP:
158-160°C
Storage:
-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
239.274g/mol
XLogP3:
3.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
239.095g/mol
Monoisotopic Mass:
239.095g/mol
Topological Polar Surface Area:
37.6A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
309
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
Undefined Atom Stereocenter Count:
0
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


The chiral compound (S)-4-(2,3-epoxypropoxy)-9H-carbazole plays a crucial role in chemical synthesis due to its unique structural features and reactivity. This compound is widely utilized as a valuable building block in the synthesis of complex organic molecules and pharmaceutical intermediates. In particular, (S)-4-(2,3-epoxypropoxy)-9H-carbazole serves as a versatile intermediate in the preparation of various functionalized carbazoles, which are important structural motifs found in a diverse range of biologically active compounds. Its ability to undergo selective transformations, such as epoxide ring-opening reactions and stereocontrolled functionalizations, makes it a valuable tool for organic chemists aiming to access enantioenriched scaffolds for further elaboration. Additionally, the presence of the carbazole core in this compound provides opportunities for further diversification through C-H activation strategies, enabling the rapid construction of molecular complexity. By incorporating (S)-4-(2,3-epoxypropoxy)-9H-carbazole into synthetic pathways, chemists can access novel chemical entities with potential applications in drug discovery, materials science, and agrochemical research.