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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)-

Silane, trimethyl-1,4-pentadiynyl-

C#CCC#C[Si](C)(C)C Request for Quotation
Chemical Name: Silane, trimethyl-1,4-pentadiynyl-
CAS Number: 71789-10-1
Product Number: AG005PTW(AGN-PC-0JMTY2)
Synonyms:
MDL No: MFCD00066350
Molecular Formula: C8H12Si
Molecular Weight: 136.2664

Identification/Properties

Computed Properties
Molecular Weight:
136.269g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
1
Exact Mass:
136.071g/mol
Monoisotopic Mass:
136.071g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
185
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:
Signal Word:
Danger
UN#:
1992
Hazard Statements:
H226-H302-H312-H315-H319-H332-H335
Precautionary Statements:
P210-P233-P240-P241-P242-P243-P260-P261-P264-P270-P271-P280-P301+P312-P302+P352-P303+P361+P353-P304-P304+P340-P305+P351+P338-P312-P321-P322-P330-P332+P313-P337+P313-P340-P362-P363-P370+P378-P403-P403+P233-P403+P235-P405-P501
Class:
3,6.1
Packing Group:
Ⅱ

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Trimethylsilyl-1,4-pentadiyne is a versatile compound widely used in organic synthesis for its unique chemical properties. This compound serves as a valuable building block in the creation of various complex organic molecules. In chemical synthesis, 1-Trimethylsilyl-1,4-pentadiyne is particularly useful as a precursor for the preparation of highly functionalized compounds through cycloaddition reactions and other transformations. Its ability to undergo selective reactions with a wide range of reagents makes it an essential tool in the development of novel organic molecules with diverse applications in pharmaceuticals, materials science, and agrochemicals. Additionally, the presence of the trimethylsilyl group enhances the stability and reactivity of 1-Trimethylsilyl-1,4-pentadiyne, making it a valuable intermediate in the synthesis of complex natural products and bioactive compounds.