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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-5-ethanesulfonamide, N-methyl-

CNS(=O)(=O)CCc1ccc2c(c1)cc[nH]2 Request for Quotation
Chemical Name: 1H-Indole-5-ethanesulfonamide, N-methyl-
CAS Number: 98623-50-8
Product Number: AG005U1Q(AGN-PC-00MPUH)
Synonyms:
MDL No:
Molecular Formula: C11H14N2O2S
Molecular Weight: 238.3061

Identification/Properties

Properties
MP:
124-125°C
BP:
458.4°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
238.305g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
238.078g/mol
Monoisotopic Mass:
238.078g/mol
Topological Polar Surface Area:
70.3A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
323
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H317
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(1H-Indol-5-yl)-N-methylethanesulfonamide is a versatile compound widely utilized in chemical synthesis for its unique properties. In the realm of organic chemistry, this specific compound serves as a valuable building block due to its ability to introduce both the indole and sulfonamide functional groups into a variety of target molecules. The presence of the indole moiety imparts aromaticity and potential for diverse reactivity, while the sulfonamide group offers a handle for further derivatization. These characteristics make 2-(1H-Indol-5-yl)-N-methylethanesulfonamide a valuable tool for the formation of complex organic structures in synthetic routes, facilitating the creation of novel compounds with potential applications in pharmaceuticals, agrochemicals, materials science, and other fields where precise chemical synthesis is paramount.