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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)-

(R)-1-(3,4-Dichlorophenyl)ethanamine hydrochloride

C[C@H](c1ccc(c(c1)Cl)Cl)N.Cl Request for Quotation
Chemical Name: (R)-1-(3,4-Dichlorophenyl)ethanamine hydrochloride
CAS Number: 1212307-96-4
Product Number: AG009ZNJ(AGN-PC-0WAM99)
Synonyms:
MDL No: MFCD12757837
Molecular Formula: C8H10Cl3N
Molecular Weight: 226.5307

Identification/Properties

Computed Properties
Molecular Weight:
226.525g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
224.988g/mol
Monoisotopic Mass:
224.988g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
129
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 (R)-1-(3,4-Dichlorophenyl)ethanamine hydrochloride is a valuable compound widely employed in chemical synthesis for its unique properties. Serving as a crucial building block in organic chemistry, this compound enables the efficient and selective formation of various complex molecules through controlled reactions. Its chiral nature, specifically its (R)-configuration, plays a vital role in directing stereochemistry during synthesis, leading to the production of enantiomerically pure compounds essential in pharmaceutical and agrochemical industries. By harnessing the reactivity of (R)-1-(3,4-Dichlorophenyl)ethanamine hydrochloride, chemists can design and construct intricate molecular structures with high precision and efficacy, ultimately advancing the frontiers of chemical research and development.