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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-imino-1-(2-phenylphenoxy)-4-piperidin-1-ylbutan-2-ol;hydrochloride

OC(CC(=N)N1CCCCC1)COc1ccccc1c1ccccc1.Cl Request for Quotation
Chemical Name: 4-imino-1-(2-phenylphenoxy)-4-piperidin-1-ylbutan-2-ol;hydrochloride
CAS Number: 179388-65-9
Product Number: AG0026ZP(AGN-PC-0MVHRO)
Synonyms:
MDL No:
Molecular Formula: C21H27ClN2O2
Molecular Weight: 374.9043

Identification/Properties

Computed Properties
Molecular Weight:
374.909g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
7
Exact Mass:
374.176g/mol
Monoisotopic Mass:
374.176g/mol
Topological Polar Surface Area:
56.6A^2
Heavy Atom Count:
26
Formal Charge:
0
Complexity:
403
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


AH 11110 hydrochloride is a versatile compound that finds wide application in chemical synthesis. This compound is commonly used as a reagent in organic chemistry reactions due to its ability to act as a catalyst in a variety of transformations. AH 11110 hydrochloride is particularly useful in the field of medicinal chemistry, where it can facilitate the creation of novel drug candidates through its unique reactivity. In addition, this compound has shown promise in the development of new materials and bioactive molecules, making it an indispensable tool for researchers in various scientific disciplines.