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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-acetonitrile

N#CCc1ccc2c(c1)cc[nH]2 Request for Quotation
Chemical Name: 1H-Indole-5-acetonitrile
CAS Number: 23690-49-5
Product Number: AG002O5Y(AGN-PC-00ORQ3)
Synonyms:
MDL No:
Molecular Formula: C10H8N2
Molecular Weight: 156.1839

Identification/Properties

Properties
MP:
58℃
BP:
374.1°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid

Safety Information

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

NMR Spectrum

Other Analytical Data

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Chemical Structure


1H-Indole-5-acetonitrile is a versatile compound commonly used in chemical synthesis as a key building block for the preparation of various pharmaceuticals, agrochemicals, and functional materials. Its unique structure and reactivity make it a valuable intermediate in the synthesis of diverse compounds.1H-Indole-5-acetonitrile serves as a precursor for the synthesis of indole derivatives, which are pivotal in medicinal chemistry due to their widespread biological activities. By undergoing various chemical transformations, this compound can be functionalized to introduce different substituents at the indole ring, allowing for the creation of novel molecules with potentially enhanced properties.Furthermore, the presence of the acetonitrile group in 1H-Indole-5-acetonitrile provides a versatile handle for further derivatization, enabling the introduction of various functional groups to tailor the compound's properties for specific applications. This flexibility makes it a valuable tool for synthetic chemists seeking to develop new compounds with desired characteristics.In summary, 1H-Indole-5-acetonitrile plays a crucial role in chemical synthesis by serving as a strategic starting material for the construction of complex molecules with diverse applications in drug discovery, agriculture, and materials science.