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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)-

1-(5-Chloro-2-fluorophenyl)ethanamine hydrochloride

Clc1ccc(c(c1)C(N)C)F.Cl Request for Quotation
Chemical Name: 1-(5-Chloro-2-fluorophenyl)ethanamine hydrochloride
CAS Number: 1955523-20-2
Product Number: AG00ASCF(AGN-PC-0WAMIW)
Synonyms:
MDL No:
Molecular Formula: C8H10Cl2FN
Molecular Weight: 210.0761

Identification/Properties

Computed Properties
Molecular Weight:
210.073g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
209.017g/mol
Monoisotopic Mass:
209.017g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
131
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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 compound 1-(5-Chloro-2-fluorophenyl)ethanamine hydrochloride, also known as $name$, serves as a versatile building block in chemical synthesis. Its unique structure, containing a substituted phenyl ring attached to an aminoethyl moiety, enables it to be used in the creation of various pharmaceuticals, agrochemicals, and other fine chemicals. In organic synthesis, this compound can undergo a range of reactions such as acylation, alkylation, and condensation, allowing for the introduction of different functional groups and the formation of complex molecules. Additionally, its halogen-substituted phenyl ring can facilitate further derivatization through cross-coupling reactions or aromatic substitutions, expanding its utility in drug discovery and material science.