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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)-

(S)-1-(4-Bromophenyl)-N-methylethanamine hydrochloride

CN[C@H](c1ccc(cc1)Br)C.Cl Request for Quotation
Chemical Name: (S)-1-(4-Bromophenyl)-N-methylethanamine hydrochloride
CAS Number: 1810074-73-7
Product Number: AG0022LS(AGN-PC-0WAMAO)
Synonyms:
MDL No:
Molecular Formula: C9H13BrClN
Molecular Weight: 250.5632

Identification/Properties

Computed Properties
Molecular Weight:
250.564g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
248.992g/mol
Monoisotopic Mass:
248.992g/mol
Topological Polar Surface Area:
12A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
108
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-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The chemical compound (S)-1-(4-Bromophenyl)-N-methylethanamine hydrochloride plays a crucial role in chemical synthesis processes due to its unique structural properties. This compound serves as a valuable intermediate in the creation of various pharmaceuticals and organic compounds. By incorporating (S)-1-(4-Bromophenyl)-N-methylethanamine hydrochloride into synthetic pathways, chemists are able to introduce specific functional groups and stereochemistry with precision. Its use in asymmetric synthesis allows for the targeted production of chiral molecules, which are essential in the pharmaceutical industry for designing drugs with enhanced efficacy and reduced side effects. Additionally, this compound can be employed in the development of novel materials and complex organic molecules, showcasing its versatility and importance in modern chemical synthesis methodologies.