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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)-

Disilane, ethynylpentamethyl-

C#C[Si]([Si](C)(C)C)(C)C Request for Quotation
Chemical Name: Disilane, ethynylpentamethyl-
CAS Number: 63247-94-9
Product Number: AG00EJC3(AGN-PC-0KS04G)
Synonyms:
MDL No:
Molecular Formula: C7H16Si2
Molecular Weight: 156.37294

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Chemical Structure


Disilane, ethynylpentamethyl-, plays a vital role in chemical synthesis as a versatile building block. Its unique chemical structure consisting of silicon and carbon atoms connected by triple bonds allows for a wide range of synthetic applications. This compound can be utilized as a cross-coupling reagent to form complex organic molecules through C-C bond formation. Additionally, Disilane, ethynylpentamethyl-, is commonly employed in the functionalization of organic substrates, enabling the introduction of specific functional groups with high selectivity. Its reactivity and compatibility with various organic reactions make it a valuable tool for the synthesis of diverse compounds in both academic research and industrial settings.