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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)-

Morpholine, 4-[(trimethylsilyl)ethynyl]-

C[Si](C#CN1CCOCC1)(C)C Request for Quotation
Chemical Name: Morpholine, 4-[(trimethylsilyl)ethynyl]-
CAS Number: 64024-63-1
Product Number: AG0036WL(AGN-PC-009QJN)
Synonyms:
MDL No:
Molecular Formula: C9H17NOSi
Molecular Weight: 183.3229

Identification/Properties

Properties
BP:
227.4°C at 760 mmHg
Storage:
Inert atmosphere;-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
183.326g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
183.108g/mol
Monoisotopic Mass:
183.108g/mol
Topological Polar Surface Area:
12.5A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
202
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


4-[(Trimethylsilyl)ethynyl]morpholine is a versatile compound commonly used in chemical synthesis for its unique properties and reactivity. In organic synthesis, it serves as a valuable building block for the construction of various complex molecules and functional materials. This compound can participate in a wide range of reactions, including cross-coupling reactions, Sonogashira couplings, and alkynylation reactions. Its trimethylsilyl-protected ethynyl group provides stability and facilitates selective transformations, making it an essential tool in the preparation of advanced organic structures. Additionally, the morpholine ring moiety in the molecule imparts favorable steric and electronic effects, enabling precise control over reactivity and selectivity in synthetic transformations. As such, 4-[(Trimethylsilyl)ethynyl]morpholine plays a crucial role in the creation of novel compounds and the development of innovative synthetic methodologies in the field of organic chemistry.