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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)-

2,3-dihydro-1H-inden-2-yl(Methyl)aMine(HCl)

CNC1Cc2c(C1)cccc2.Cl Request for Quotation
Chemical Name: 2,3-dihydro-1H-inden-2-yl(Methyl)aMine(HCl)
CAS Number: 10408-85-2
Product Number: AG008SSX(AGN-PC-0WA5KI)
Synonyms:
MDL No:
Molecular Formula: C10H14ClN
Molecular Weight: 183.6779

Identification/Properties

Computed Properties
Molecular Weight:
183.679g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
183.081g/mol
Monoisotopic Mass:
183.081g/mol
Topological Polar Surface Area:
12A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
119
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-Methyl-2,3-dihydro-1H-inden-2-amine hydrochloride is a versatile compound widely used in chemical synthesis as a key intermediate in the production of various pharmaceuticals and fine chemicals. Due to its unique molecular structure, this compound serves as a valuable building block for the synthesis of complex organic molecules with important biological activities.In organic synthesis, N-Methyl-2,3-dihydro-1H-inden-2-amine hydrochloride can participate in a variety of reactions such as alkylation, acylation, and cyclization to create new carbon-carbon and carbon-nitrogen bonds. Its reactivity and stability make it an excellent choice for the preparation of structurally diverse compounds with potential therapeutic applications.Researchers and chemists utilize N-Methyl-2,3-dihydro-1H-inden-2-amine hydrochloride to access novel chemical structures that can be further optimized for drug discovery and development. By incorporating this intermediate into their synthetic routes, they can efficiently construct complex molecules with precise stereochemistry and functional group tolerance.In summary, N-Methyl-2,3-dihydro-1H-inden-2-amine hydrochloride plays a crucial role in the modern chemical synthesis of biologically active compounds, offering chemists a powerful tool for the creation of innovative pharmaceuticals and materials.