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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)-

Piperidine, 4-(3-chlorophenoxy)-

Clc1cccc(c1)OC1CCNCC1 Request for Quotation
Chemical Name: Piperidine, 4-(3-chlorophenoxy)-
CAS Number: 97840-40-9
Product Number: AG003K10(AGN-PC-0KK70L)
Synonyms:
MDL No:
Molecular Formula: C11H14ClNO
Molecular Weight: 211.6880

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
211.689g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
211.076g/mol
Monoisotopic Mass:
211.076g/mol
Topological Polar Surface Area:
21.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
171
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

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(3-Chlorophenoxy)piperidine is a versatile compound that finds wide application in chemical synthesis due to its unique properties and reactivity. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its presence of both a piperidine ring and a chlorophenyl group confers it with different avenues for chemical modifications, making it a valuable intermediate in organic synthesis. Chemists commonly utilize 4-(3-Chlorophenoxy)piperidine in the development of new drug candidates and in the production of fine chemicals with diverse functionalities. Its ability to undergo different reactions such as nucleophilic substitutions, metal-catalyzed couplings, and functional group transformations makes it a valuable tool for achieving complex molecular structures in chemical synthesis.