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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)-

3-Ethynylpiperidine hydrochloride

C#CC1CCCNC1.Cl Request for Quotation
Chemical Name: 3-Ethynylpiperidine hydrochloride
CAS Number: 959918-19-5
Product Number: AG0069NK(AGN-PC-09RMP0)
Synonyms:
MDL No:
Molecular Formula: C7H12ClN
Molecular Weight: 145.6299

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
145.63g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
145.066g/mol
Monoisotopic Mass:
145.066g/mol
Topological Polar Surface Area:
12A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
109
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


3-Ethynylpiperidine hydrochloride is a versatile chemical compound commonly utilized in the field of chemical synthesis for its unique properties and reactivity. As a key building block in organic chemistry, this compound serves as a valuable intermediate in the production of various pharmaceuticals, agrochemicals, and fine chemicals.One prominent application of 3-Ethynylpiperidine hydrochloride is its role as a precursor in the synthesis of heterocyclic compounds, particularly in the formation of complex ring structures. Its alkynyl functional group enables the introduction of this moiety into target molecules, allowing for the creation of diverse chemical structures with specific properties and functionalities.Furthermore, the presence of the piperidine ring in this compound lends itself to the development of biologically active compounds, making it a valuable starting material in medicinal chemistry research. By incorporating 3-Ethynylpiperidine hydrochloride into drug synthesis pathways, chemists can access a wide range of potential pharmaceutical candidates with improved pharmacological profiles and therapeutic benefits.Overall, the strategic use of 3-Ethynylpiperidine hydrochloride in chemical synthesis offers a pathway to the efficient and selective construction of complex molecules with tailored properties, making it an indispensable tool for advancing the frontiers of modern organic chemistry.