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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)-

Benzeneethanamine, N,N-dimethyl-, hydrochloride

CN(CCc1ccccc1)C.Cl Request for Quotation
Chemical Name: Benzeneethanamine, N,N-dimethyl-, hydrochloride
CAS Number: 10275-21-5
Product Number: AG0008AM(AGN-PC-0JKI0V)
Synonyms:
MDL No:
Molecular Formula: C10H16ClN
Molecular Weight: 185.6937

Identification/Properties

Computed Properties
Molecular Weight:
185.695g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
3
Exact Mass:
185.097g/mol
Monoisotopic Mass:
185.097g/mol
Topological Polar Surface Area:
3.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
93
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Benzeneethanamine, N,N-dimethyl-, hydrochloride (1:1) is commonly utilized in chemical synthesis as a versatile intermediate compound. The presence of the hydrochloride salt helps to enhance the solubility and stability of the molecule, making it especially valuable in organic reactions. Its amine functional group allows for a range of transformations, such as nucleophilic substitution, reductive amination, and condensation reactions, facilitating the synthesis of various complex organic compounds. This compound serves as a crucial building block in the development of pharmaceuticals, agrochemicals, and specialty chemicals due to its reactivity and compatibility with a variety of reaction conditions.