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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)-

2-Propyn-1-amine, N,N-diethyl-

CCN(CC#C)CC Request for Quotation
Chemical Name: 2-Propyn-1-amine, N,N-diethyl-
CAS Number: 4079-68-9
Product Number: AG003SJZ(AGN-PC-0JKF0X)
Synonyms:
MDL No:
Molecular Formula: C7H13N
Molecular Weight: 111.1848

Identification/Properties

Properties
MP:
157-161°C
BP:
118-120 °C(lit.)
Storage:
Room Temperature;
Form:
Liquid
Stability:
Air & Light Sensitive
Refractive Index:
n20/D 1.434
Computed Properties
Molecular Weight:
111.188g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
3
Exact Mass:
111.105g/mol
Monoisotopic Mass:
111.105g/mol
Topological Polar Surface Area:
3.2A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
83.8
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


N,N-Diethylpropargylamine is a versatile chemical compound that finds widespread application in organic synthesis reactions. This amine compound serves as an effective reagent in various chemical transformations, particularly in the formation of complex organic molecules. Through its unique chemical properties, N,N-Diethylpropargylamine contributes to the creation of new carbon-carbon bonds and facilitates the synthesis of valuable intermediates for pharmaceuticals, agrochemicals, and other fine chemicals. Its ability to participate in a variety of reactions, such as nucleophilic addition, alkylation, and elimination, makes it a valuable tool for organic chemists seeking to access diverse molecular structures efficiently. Additionally, N,N-Diethylpropargylamine can act as a ligand in transition metal-catalyzed reactions, enhancing the selectivity and efficiency of certain transformations. This compound's versatility and reactivity make it a valuable asset in modern organic synthesis strategies, allowing chemists to explore novel pathways for the construction of complex molecules.