1. Home
  2. Silane, chlorodimethyl(pentafluorophenyl)-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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, chlorodimethyl(pentafluorophenyl)-

Fc1c(F)c(F)c(c(c1F)[Si](Cl)(C)C)F Request for Quotation
Chemical Name: Silane, chlorodimethyl(pentafluorophenyl)-
CAS Number: 20082-71-7
Product Number: AG002D1W(AGN-PC-0JLXDF)
Synonyms:
MDL No:
Molecular Formula: C8H6ClF5Si
Molecular Weight: 260.6638

Identification/Properties

Computed Properties
Molecular Weight:
260.663g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
259.985g/mol
Monoisotopic Mass:
259.985g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
223
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

Request for Quotation

Customer Feedback

Chemical Structure


Chlorodimethyl(pentafluorophenyl)silane is a versatile organosilane compound that finds wide applications in various chemical synthesis processes. It serves as a valuable reagent in the introduction of pentafluorophenyl groups into organic molecules, offering a unique way to modify the properties of compounds for specific purposes. This compound is commonly used as a silylating agent, enabling the selective protection of hydroxyl groups in complex organic molecules. By utilizing Chlorodimethyl(pentafluorophenyl)silane in silylation reactions, chemists can facilitate multi-step synthesis pathways by controlling the reactivity of functional groups, thus enhancing the efficiency of the overall synthetic process. Additionally, Chlorodimethyl(pentafluorophenyl)silane is employed in the preparation of organosilicon compounds for use in materials science and pharmaceutical research. Its ability to introduce pentafluorophenyl functionalities into silicon-based materials allows for the development of novel structures with tailored properties, making it a valuable tool for designing advanced materials with specific applications. Overall, Chlorodimethyl(pentafluorophenyl)silane plays a crucial role in chemical synthesis by enabling precise modifications of organic molecules and facilitating the creation of new materials with enhanced properties. Its versatility and utility make it a valuable component in the toolkit of synthetic chemists working in various fields.