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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)-

4-(tetrahydropyran-4-yloxy)aniline

Nc1ccc(cc1)OC1CCOCC1 Request for Quotation
Chemical Name: 4-(tetrahydropyran-4-yloxy)aniline
CAS Number: 917483-71-7
Product Number: AG00GVQI(AGN-PC-04G0L1)
Synonyms:
MDL No:
Molecular Formula: C11H15NO2
Molecular Weight: 193.2423

Identification/Properties

Properties
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(Tetrahydropyran-4-yloxy)aniline, also known as THP-aniline, serves as a versatile building block in chemical synthesis. This compound finds widespread application as a protecting group in organic chemistry reactions. By selectively masking the amino group (-NH2) with the tetrahydropyran (THP) moiety, THP-aniline helps to control reactivity and regioselectivity in various synthetic transformations. This protection strategy enables chemists to carry out specific reactions without interference from other functional groups present in the molecule. THP-aniline's ease of installation and removal under mild conditions makes it a valuable tool in the synthesis of complex organic molecules, pharmaceuticals, and materials. Its broad applicability underscores its importance as a valuable reagent in modern organic synthesis.