1. Home
  2. 1-(6-amino-5-methoxy-2,3-dihydroindol-1-yl)ethanone

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

1-(6-amino-5-methoxy-2,3-dihydroindol-1-yl)ethanone

COc1cc2CCN(c2cc1N)C(=O)C Request for Quotation
Chemical Name: 1-(6-amino-5-methoxy-2,3-dihydroindol-1-yl)ethanone
CAS Number: 23772-41-0
Product Number: AG006UKU(AGN-PC-0CXYCU)
Synonyms:
MDL No:
Molecular Formula: C11H14N2O2
Molecular Weight: 206.2411

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
206.245g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
206.106g/mol
Monoisotopic Mass:
206.106g/mol
Topological Polar Surface Area:
55.6A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
257
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

Request for Quotation

Customer Feedback

Chemical Structure


The compound 1-(6-Amino-5-methoxyindolin-1-yl)ethanone, also known as $name$, is a versatile building block widely used in chemical synthesis. This compound plays a crucial role in the development of pharmaceuticals, agrochemicals, and materials science through its diverse applications across organic chemistry.$name$ is an important intermediate in the synthesis of various bioactive heterocyclic compounds and natural products. Its unique structure containing an amino group, a methoxy group, and an indolin-2-one moiety provides ample opportunities for functionalization and derivatization, making it a valuable tool for modifying molecular structures and designing new molecules with desired properties.In chemical synthesis, $name$ serves as a key precursor for the preparation of indole-based derivatives, which are frequently encountered in drug discovery and the synthesis of biologically active molecules. Its ability to participate in cross-coupling reactions, cyclization processes, and other transformations enables chemists to access a broad range of target molecules efficiently and selectively.Moreover, the presence of both electron-rich and electron-deficient functional groups in $name$ facilitates its involvement in various synthetic strategies, such as nucleophilic addition, electrophilic substitution, and reductive amination. This versatility allows researchers to tailor the structure and properties of the final products for specific applications in medicinal chemistry, crop protection, and material science.Overall, the strategic importance of 1-(6-Amino-5-methoxyindolin-1-yl)ethanone in chemical synthesis lies in its utility as a versatile starting material for the construction of complex organic molecules with potential biological activities and functional properties. By harnessing its synthetic potential, chemists can explore new pathways for creating innovative compounds that may lead to advancements in various scientific fields.