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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)-

1-Methylazepan-4-amine

CN1CCCC(CC1)N Request for Quotation
Chemical Name: 1-Methylazepan-4-amine
CAS Number: 933741-93-6
Product Number: AG00IHKZ(AGN-PC-09LIV2)
Synonyms:
MDL No:
Molecular Formula: C7H16N2
Molecular Weight: 128.2153

Identification/Properties

Computed Properties
Molecular Weight:
128.219g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
128.131g/mol
Monoisotopic Mass:
128.131g/mol
Topological Polar Surface Area:
29.3A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
83
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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

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Chemical Structure


1-Methylazepan-4-amine, also known as N-methylazepan-4-amine, is a valuable building block in chemical synthesis. Its unique chemical structure and properties make it a versatile compound used in various organic reactions and transformations.In chemical synthesis, 1-Methylazepan-4-amine serves as a key intermediate in the preparation of a wide range of pharmaceuticals, agrochemicals, and specialty chemicals. Its cyclic amine structure allows for selective functionalization at different positions, enabling the synthesis of complex molecules with specific biological activities.One common application of 1-Methylazepan-4-amine is in the synthesis of heterocyclic compounds, where it can participate in ring-forming reactions to create fused ring systems found in many biologically active molecules. Additionally, its amine group can serve as a nucleophile in various coupling reactions, facilitating the introduction of diverse functional groups into target compounds.Overall, the strategic incorporation of 1-Methylazepan-4-amine into synthetic pathways enables chemists to access structurally diverse and biologically relevant compounds, making it a valuable tool in chemical synthesis.