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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-(2-methoxyethyl)piperidine;hydrochloride

COCCC1CCNCC1.Cl Request for Quotation
Chemical Name: 4-(2-methoxyethyl)piperidine;hydrochloride
CAS Number: 868849-54-1
Product Number: AG00IE8Y(AGN-PC-03YOGC)
Synonyms:
MDL No:
Molecular Formula: C8H18ClNO
Molecular Weight: 179.6876

Identification/Properties

Computed Properties
Molecular Weight:
179.688g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
179.108g/mol
Monoisotopic Mass:
179.108g/mol
Topological Polar Surface Area:
21.3A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
79.3
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:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(2-Methoxyethyl)piperidine hydrochloride is a versatile compound widely used in chemical synthesis for its unique properties. In organic chemistry, it serves as a crucial building block in the production of various pharmaceuticals and agrochemicals. This compound is particularly valued for its ability to introduce the piperidine ring structure into complex molecules, making it an essential component in the synthesis of diverse chemical compounds. Additionally, its hydrochloride salt form enhances its solubility in water, facilitating its use in a wide range of aqueous-based reactions. Furthermore, the methoxyethyl group attached to the piperidine ring provides increased stability and selectivity in organic reactions, making it a valuable tool for chemists in designing and synthesizing novel compounds with specific properties and functionalities.