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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)-

8-Azabicyclo[3.2.1]octan-3-amine, 8-methyl-

NC1C[C@@H]2CC[C@H](C1)N2C Request for Quotation
Chemical Name: 8-Azabicyclo[3.2.1]octan-3-amine, 8-methyl-
CAS Number: 98998-25-5
Product Number: AG0039AF(AGN-PC-0JQSJJ)
Synonyms:
MDL No:
Molecular Formula: C8H16N2
Molecular Weight: 140.2260

Identification/Properties

Computed Properties
Molecular Weight:
140.23g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
140.131g/mol
Monoisotopic Mass:
140.131g/mol
Topological Polar Surface Area:
29.3A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
121
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
2
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


3-Aminotropane, also known as 3-AT, is a versatile compound commonly used in chemical synthesis due to its unique properties and reactivity. As a primary amine, 3-Aminotropane serves as a valuable building block in the creation of various complex chemicals and pharmaceuticals. Its structure enables it to participate in a wide range of reactions, making it a valuable tool for chemists looking to create new molecules with specific functionalities.In chemical synthesis, 3-Aminotropane can be utilized as a key intermediate in the production of numerous important compounds. It can undergo various reactions such as condensation, hydrogenation, and alkylation to introduce different functional groups onto its molecule. This versatility allows chemists to tailor the properties of the final product to meet specific requirements.One common application of 3-Aminotropane is in the synthesis of heterocyclic compounds, which are widely used in the pharmaceutical industry. By reacting 3-Aminotropane with suitable reagents, chemists can access a diverse array of heterocycles with desired pharmacological activities. Additionally, 3-Aminotropane can serve as a precursor for the synthesis of various amine derivatives, which find applications in materials science, agrochemicals, and other industries.Overall, 3-Aminotropane plays a crucial role in chemical synthesis by providing a versatile platform for the construction of complex molecules with tailored properties. Its ease of modification and wide range of applications make it an indispensable tool for chemists striving to innovate and develop novel compounds for diverse purposes.