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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)-

5-chloropent-4-ynyl(triethyl)silane

ClCCCC#C[Si](CC)(CC)CC Request for Quotation
Chemical Name: 5-chloropent-4-ynyl(triethyl)silane
CAS Number: 174125-30-5
Product Number: AG001ZH4(AGN-PC-00UQGR)
Synonyms:
MDL No:
Molecular Formula: C11H21ClSi
Molecular Weight: 216.8229

Identification/Properties

Computed Properties
Molecular Weight:
216.824g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
6
Exact Mass:
216.11g/mol
Monoisotopic Mass:
216.11g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
175
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


Silane, (5-chloro-1-pentyn-1-yl)triethyl-, is a versatile chemical compound commonly used in chemical synthesis processes. Its application in organic synthesis lies in its ability to function as a key building block for the synthesis of various organic molecules with unique properties. The presence of the chloro and alkynyl groups in the molecule allows for diverse functionalization and modification reactions, enabling the creation of complex organic structures. This compound can serve as a valuable reagent in the production of pharmaceuticals, agrochemicals, and materials with specific functionalities. Additionally, the triethylsilane moiety provides stability and compatibility in various reaction conditions, making it a valuable tool for chemists involved in the design and development of novel compounds.