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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)-

(1R)-1-(2-fluoro-5-methoxyphenyl)ethylamine

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Chemical Name: (1R)-1-(2-fluoro-5-methoxyphenyl)ethylamine
CAS Number: 1213670-08-6
Product Number: AG009G4U(AGN-PC-0WAL45)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

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Chemical Structure


The chiral compound (R)-1-(2-Fluoro-5-methoxyphenyl)ethan-1-amine plays a crucial role in chemical synthesis as a versatile building block. With its unique structure and stereochemistry, this compound is valued for its ability to be incorporated into various organic molecules, enabling the synthesis of complex pharmaceuticals, agrochemicals, and materials. Its presence in a synthesis pathway can impart specific biological activities or enhance the desired properties of the final product. Additionally, the stereochemical purity of (R)-1-(2-Fluoro-5-methoxyphenyl)ethan-1-amine is essential in asymmetric synthesis, where the control of chirality is critical for obtaining the desired enantiomeric excess in the final compound. This compound's potential applications extend across multiple fields of chemistry, making it a valuable tool for researchers and synthetic chemists seeking to design and create new molecules with tailored properties and functions.