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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-Butanamine, 2,3-dimethyl-

NCC(C(C)C)C Request for Quotation
Chemical Name: 1-Butanamine, 2,3-dimethyl-
CAS Number: 66553-05-7
Product Number: AG006KOZ(AGN-PC-02KL23)
Synonyms:
MDL No:
Molecular Formula: C6H15N
Molecular Weight: 101.1900

Identification/Properties

Computed Properties
Molecular Weight:
101.193g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
101.12g/mol
Monoisotopic Mass:
101.12g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
41.4
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


2,3-Dimethylbutan-1-amine is a versatile compound widely used in chemical synthesis as a key intermediate in the production of various pharmaceuticals, agrochemicals, and industrial chemicals. Its unique molecular structure allows for a range of transformations and functional group manipulations, making it a valuable building block in organic synthesis.One of the primary applications of 2,3-Dimethylbutan-1-amine is as a precursor in the synthesis of various heterocyclic compounds, particularly in the development of new drug candidates. By utilizing its amine functionality, this compound can participate in a variety of reactions such as nucleophilic substitution, reductive amination, and transition metal-catalyzed coupling reactions to introduce diverse chemical functionalities into the desired molecules.Furthermore, 2,3-Dimethylbutan-1-amine can also serve as a chiral auxiliary in asymmetric synthesis, enabling the creation of enantiopure compounds with high stereochemical control. Its presence in the molecule can influence the stereochemistry of subsequent reactions, leading to the selective formation of specific stereoisomers.Overall, the versatile nature of 2,3-Dimethylbutan-1-amine makes it a valuable tool in the hands of synthetic chemists for the efficient and selective construction of complex organic molecules with diverse applications.