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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-methyl-1,4-oxazepan-6-yl)methyl]amine dihydrochloride

NCC1COCCN(C1)C.Cl.Cl Request for Quotation
Chemical Name: [(4-methyl-1,4-oxazepan-6-yl)methyl]amine dihydrochloride
CAS Number: 1609400-87-4
Product Number: AG00J2A1(AGN-PC-0WB7AS)
Synonyms:
MDL No: MFCD26959708
Molecular Formula: C7H18Cl2N2O
Molecular Weight: 217.1366

Identification/Properties

Computed Properties
Molecular Weight:
217.134g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
216.08g/mol
Monoisotopic Mass:
216.08g/mol
Topological Polar Surface Area:
38.5A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
97.6
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:
3
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


1,4-Oxazepine-6-methanamine, hexahydro-4-methyl-, hydrochloride (1:2) is a valuable compound in chemical synthesis. This specific compound is commonly used as a versatile building block for the preparation of various pharmaceuticals and organic molecules. It serves as a key intermediate in the synthesis of complex organic compounds due to its structural reactivity and functional groups.In chemical synthesis, 1,4-Oxazepine-6-methanamine, hexahydro-4-methyl-, hydrochloride (1:2) can be utilized as a precursor for the creation of biologically active compounds, such as potential drug candidates or intermediates for pharmaceutical research. Its unique structure allows for efficient manipulation in synthetic pathways, enabling the introduction of specific functional groups or stereochemistry required for the desired end product.Furthermore, this compound can participate in diverse chemical reactions including acylation, alkylation, and nucleophilic substitution, expanding its utility in building complex molecular architectures. Its compatibility with various synthetic methodologies makes it a valuable tool for organic chemists seeking to design and prepare novel compounds with specific properties or biological activities.