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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)-

Pyridine, 2-chloro-5-[(trimethylsilyl)ethynyl]-

Clc1ccc(cn1)C#C[Si](C)(C)C Request for Quotation
Chemical Name: Pyridine, 2-chloro-5-[(trimethylsilyl)ethynyl]-
CAS Number: 263012-81-3
Product Number: AG002SMI(AGN-PC-0N7VLO)
Synonyms:
MDL No:
Molecular Formula: C10H12ClNSi
Molecular Weight: 209.7475

Identification/Properties

Properties
MP:
58-59℃
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
209.748g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
209.043g/mol
Monoisotopic Mass:
209.043g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
232
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

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Chloro-5-((trimethylsilyl)ethynyl)pyridine is a versatile compound widely used in chemical synthesis due to its unique reactivity and structural properties. In organic chemistry, it serves as a valuable building block for the preparation of various functionalized organic molecules. This compound undergoes substitution reactions to introduce the pyridine ring into various organic frameworks, allowing for the formation of complex structures with diverse functionalities. Additionally, 2-Chloro-5-((trimethylsilyl)ethynyl)pyridine can serve as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and materials with tailored properties. Its ability to participate in cross-coupling reactions and other transformations makes it a valuable tool for organic chemists seeking to access novel compounds with potential applications in drug discovery, materials science, and other fields.