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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-(4-Fluoro-3-methoxyphenyl)ethylamine HCl

COc1cc(ccc1F)[C@H](N)C Request for Quotation
Chemical Name: (1R)-1-(4-Fluoro-3-methoxyphenyl)ethylamine HCl
CAS Number: 1157581-09-3
Product Number: AG000GTM(AGN-PC-0WA1NO)
Synonyms:
MDL No:
Molecular Formula: C9H12FNO
Molecular Weight: 169.1961

Identification/Properties

Computed Properties
Molecular Weight:
169.199g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
169.09g/mol
Monoisotopic Mass:
169.09g/mol
Topological Polar Surface Area:
35.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
143
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:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
2735
Hazard Statements:
H302-H318
Precautionary Statements:
P280-P305+P351+P338
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


(R)-1-(4-Fluoro-3-methoxyphenyl)ethanamine, also known as the chiral amine, is a valuable compound in chemical synthesis due to its versatile applications. This compound plays a crucial role as a chiral building block in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Its enantiomeric purity is particularly important in asymmetric synthesis, where it serves as a key starting material for the preparation of enantiopure compounds. Additionally, (R)-1-(4-Fluoro-3-methoxyphenyl)ethanamine can be utilized in the development of new materials and as a catalyst in asymmetric reactions, offering a greener and more efficient approach to synthesizing complex molecules.