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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-(2-Bromophenyl)ethanamine hydrochloride

C[C@@H](c1ccccc1Br)N.Cl Request for Quotation
Chemical Name: (S)-1-(2-Bromophenyl)ethanamine hydrochloride
CAS Number: 1187931-26-5
Product Number: AG008Z4T(AGN-PC-0WAMD3)
Synonyms:
MDL No: MFCD09997783
Molecular Formula: C8H11BrClN
Molecular Weight: 236.5366

Identification/Properties

Computed Properties
Molecular Weight:
236.537g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
234.976g/mol
Monoisotopic Mass:
234.976g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
105
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


(S)-1-(2-Bromophenyl)ethanamine hydrochloride, commonly used in chemical synthesis, serves as a versatile building block with significant applications. Its chiral nature makes it a valuable tool in the production of optically pure compounds, particularly in the pharmaceutical industry where enantiopurity is crucial. This compound can be employed as a key intermediate in the synthesis of various biologically active molecules, including pharmaceuticals, agrochemicals, and functional materials. By incorporating (S)-1-(2-Bromophenyl)ethanamine hydrochloride into synthetic routes, chemists can access a wide range of stereochemically complex structures with high enantiomeric purity, enabling the development of novel compounds with enhanced pharmacological or biological properties.