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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)-

4-methoxy-2,3-dihydro-1H-indole;hydrochloride

COc1cccc2c1CCN2.Cl Request for Quotation
Chemical Name: 4-methoxy-2,3-dihydro-1H-indole;hydrochloride
CAS Number: 90609-70-4
Product Number: AG006C6C(AGN-PC-07HAXO)
Synonyms:
MDL No:
Molecular Formula: C9H12ClNO
Molecular Weight: 185.6507

Identification/Properties

Properties
MP:
202℃
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
185.651g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
185.061g/mol
Monoisotopic Mass:
185.061g/mol
Topological Polar Surface Area:
21.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
138
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Methoxyindoline hydrochloride, a versatile chemical compound, serves as a valuable reagent in organic and medicinal chemistry. Its application in chemical synthesis is well-recognized, particularly in the development of pharmaceuticals and novel organic molecules. By serving as a key intermediate in various reactions, 4-Methoxyindoline hydrochloride facilitates the creation of complex molecular structures with precision and efficiency. Its unique properties contribute significantly to the synthesis of biologically active compounds, enabling researchers to explore new avenues in drug discovery and material science. When used judiciously in synthesis processes, this compound offers a wide range of possibilities for designing innovative molecules with specific functions and applications.