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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-chlorophenyl)-, hydrochloride

Clc1cccc(c1)C1CCNCC1.Cl Request for Quotation
Chemical Name: Piperidine, 4-(3-chlorophenyl)-, hydrochloride
CAS Number: 99329-70-1
Product Number: AG005SQJ(AGN-PC-079VBA)
Synonyms:
MDL No:
Molecular Formula: C11H15Cl2N
Molecular Weight: 232.1495

Identification/Properties

Properties
BP:
324 °C at 760 mmHg
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
232.148g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
231.058g/mol
Monoisotopic Mass:
231.058g/mol
Topological Polar Surface Area:
12A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
154
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Piperidine, 4-(3-chlorophenyl)-, hydrochloride (1:1) is a versatile chemical reagent commonly employed in chemical synthesis processes. Its applications in organic chemistry are extensive, as it serves as a crucial building block for the creation of various pharmaceuticals, agrochemicals, and fine chemicals. The presence of the 3-chlorophenyl moiety introduces specific reactivity and selectivity to reactions, allowing for the formation of unique chemical structures. This compound is particularly valuable in the formation of heterocyclic compounds and complex organic molecules. Additionally, its hydrochloride form enhances its solubility and stability, making it easier to handle in laboratory settings. Overall, Piperidine, 4-(3-chlorophenyl)-, hydrochloride plays a pivotal role in advancing the field of chemical synthesis by enabling the efficient and precise construction of intricate chemical compounds.