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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)-

Benzenamine, 3-fluoro-4-(4-morpholinyl)-

Nc1ccc(c(c1)F)N1CCOCC1 Request for Quotation
Chemical Name: Benzenamine, 3-fluoro-4-(4-morpholinyl)-
CAS Number: 93246-53-8
Product Number: AG0033PB(AGN-PC-077VCV)
Synonyms:
MDL No: MFCD02571270
Molecular Formula: C10H13FN2O
Molecular Weight: 196.2214

Identification/Properties

Properties
MP:
121-123°C
BP:
364.9°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
196.225g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
196.101g/mol
Monoisotopic Mass:
196.101g/mol
Topological Polar Surface Area:
38.5A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
185
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Fluoro-4-morpholinoaniline is a versatile chemical compound widely used in chemical synthesis due to its unique properties and reactivity. This compound serves as a valuable building block in the production of various pharmaceuticals, agrochemicals, and organic materials. In chemical synthesis, 3-Fluoro-4-morpholinoaniline functions as a key intermediate in the creation of complex molecules and organic compounds. Its fluorine substituent provides specific steric and electronic properties that can be exploited to influence the overall reactivity and selectivity of chemical reactions. One of the primary applications of 3-Fluoro-4-morpholinoaniline is in the synthesis of pharmaceutical agents, where its presence can enhance the biological activity and pharmacokinetic properties of the final drug molecules. Additionally, this compound can be used in the development of novel materials with tailored properties for various industrial applications.Overall, 3-Fluoro-4-morpholinoaniline plays a crucial role in advancing the field of chemical synthesis by enabling the efficient preparation of diverse compounds with enhanced properties and functionalities.