Welcome to LookChem.com Sign In|Join Free
  • or
Cyclohex-2-enyltriphenylsilane is an organosilicon compound with the chemical formula C24H25Si. It is a colorless to pale yellow solid, soluble in common organic solvents such as dichloromethane, tetrahydrofuran, and toluene. cyclohex-2-enyltriphenylsilane is characterized by a cyclohexene ring with a double bond at the 2-position, and three phenyl groups attached to a silicon atom. Cyclohex-2-enyltriphenylsilane is primarily used as a reagent in organic synthesis, particularly in the formation of carbon-carbon bonds through the Peterson olefination reaction. It is also employed as a ligand in transition metal-catalyzed reactions and as a precursor for the synthesis of other organosilicon compounds. Due to its stability and reactivity, cyclohex-2-enyltriphenylsilane has found applications in various fields, including pharmaceuticals, materials science, and the development of new synthetic methodologies.

1829-57-8

Post Buying Request

1829-57-8 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1829-57-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1829-57-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,2 and 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1829-57:
(6*1)+(5*8)+(4*2)+(3*9)+(2*5)+(1*7)=98
98 % 10 = 8
So 1829-57-8 is a valid CAS Registry Number.

1829-57-8Relevant academic research and scientific papers

Ene Reactions of Allylic Derivatives of Silicon, Germanium, Tin and Lead with N-Phenyltriazolinedione: the Effect of Varying the Metal

Cai, Jiaqiang,Davies, Alwyn G.

, p. 1743 - 1746 (2007/10/02)

The compounds Ph3MCH2CH=CH2 and (M=Si, Ge, Sn or Pb) have been treated with 4-phenyl-1,2,4-triazoline-3,5-dione, and the relative yields of the products of the M-ene reaction, of the H-ene reaction, and of the reaction involving cycloaddition with shift of the organometallic substituent, have been determined.The silicon compounds react principally by the H-ene process.The cycloaddition process is at a maximum (50percent or 70percent) with the germanium compounds, and the tin compounds show mainly the M-ene reaction, with some cycloaddition but no H-ene reaction.Triphenylprop-2-enylplumbane show only the M-ene reaction.In trimethyl(1,1-dimethylprop-2-enyl)silane, in which the H-ene reaction is blocked, only cycloaddition with shift of the silyl group is observed.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 1829-57-8