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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)-

1H-Indole-3-carboxamide, N-(2-chlorophenyl)-

Clc1ccccc1NC(=O)c1c[nH]c2c1cccc2 Request for Quotation
Chemical Name: 1H-Indole-3-carboxamide, N-(2-chlorophenyl)-
CAS Number: 61788-27-0
Product Number: AG00F4Z7(AGN-PC-0NIT3J)
Synonyms:
MDL No:
Molecular Formula: C15H11ClN2O
Molecular Weight: 270.7136

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Computed Properties
Molecular Weight:
270.716g/mol
XLogP3:
3.9
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
270.056g/mol
Monoisotopic Mass:
270.056g/mol
Topological Polar Surface Area:
44.9A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
336
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
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


N-(2-Chlorophenyl)-1H-indole-3-carboxamide, also known as $name$, is a versatile chemical compound widely used in organic synthesis. In the field of chemical synthesis, this compound serves as a valuable building block for the construction of various complex molecules. Its broad applicability stems from its ability to participate in a range of important reactions, making it a crucial component in the development of new chemical entities.One key application of N-(2-Chlorophenyl)-1H-indole-3-carboxamide is in the synthesis of pharmaceutical compounds. By incorporating this compound into synthetic routes, chemists can access novel drug candidates with enhanced biological activity and pharmacological properties. Furthermore, its unique indole core structure grants it the potential to target specific biological pathways, making it a valuable tool in drug discovery research.Moreover, N-(2-Chlorophenyl)-1H-indole-3-carboxamide is utilized in the preparation of functional materials and organic dyes. Its structural features allow for the modification of its chemical properties, enabling the creation of tailor-made molecules for various applications such as organic electronics, sensors, and materials science.Overall, the versatility and reactivity of N-(2-Chlorophenyl)-1H-indole-3-carboxamide make it a cornerstone in the toolkit of synthetic chemists seeking to develop innovative compounds for pharmaceuticals, materials, and other specialized applications.