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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-Butanamine, 3,3-dimethyl-, hydrochloride, (2S)-

C[C@@H](C(C)(C)C)N.Cl Request for Quotation
Chemical Name: 2-Butanamine, 3,3-dimethyl-, hydrochloride, (2S)-
CAS Number: 31519-55-8
Product Number: AG003A29(AGN-PC-0O8UDO)
Synonyms:
MDL No:
Molecular Formula: C6H16ClN
Molecular Weight: 137.6509

Identification/Properties

Computed Properties
Molecular Weight:
137.651g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
137.097g/mol
Monoisotopic Mass:
137.097g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
51.7
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-3,3-Dimethylbutan-2-amine hydrochloride, also known as $name$, is a versatile compound widely used in chemical synthesis. As a chiral amine compound, it plays a crucial role in asymmetric synthesis, particularly in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its chiral nature allows for the selective formation of enantiomerically pure products, making it valuable in the development of new drugs and other high-value compounds. Additionally, (S)-3,3-Dimethylbutan-2-amine hydrochloride can act as a catalyst or reagent in various reactions, enabling the creation of complex molecular structures with high efficiency and precision. Its application in chemical synthesis provides chemists with a powerful tool to access a wide range of stereochemically diverse compounds with enhanced biological activity and industrial applications.