Welcome to LookChem.com Sign In|Join Free
  • or
Trimethyl(phenyl)methylthiomethylsilane is an organosilicon compound characterized by its unique structure, which consists of a silicon atom bonded to three methyl groups and a phenyl group attached to a methylthiomethyl moiety. trimethyl<<(phenyl)methyl>thiomethyl>silane is often used as a reagent in organic synthesis, particularly in the formation of carbon-sulfur bonds. It is known for its ability to act as a silylating agent, facilitating various chemical transformations. The phenyl group provides steric hindrance, which can influence the reactivity and selectivity of the compound in reactions. Trimethyl(phenyl)methylthiomethylsilane is also recognized for its potential applications in the synthesis of pharmaceuticals and other specialty chemicals, where its specific structural features can be leveraged to achieve desired chemical outcomes.

17988-38-4

Post Buying Request

17988-38-4 Suppliers

Recommended suppliers

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

17988-38-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17988-38-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,8 and 8 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 17988-38:
(7*1)+(6*7)+(5*9)+(4*8)+(3*8)+(2*3)+(1*8)=164
164 % 10 = 4
So 17988-38-4 is a valid CAS Registry Number.

17988-38-4Relevant academic research and scientific papers

Strategic Trimethylsilyldiazomethane Insertion into pinB-SR Followed by Selective Alkylations

Civit, Marc G.,Royes, Jordi,Vogels, Christopher M.,Westcott, Stephen A.,Cuenca, Ana B.,Fernández, Elena

supporting information, p. 3830 - 3833 (2016/08/16)

The insertion of the diazo derivative Me3SiCHN2 into pinB-SR σ bonds (R = Ph, Tol, Bn) allows a direct synthesis of multisubstituted H-C(SR)(Bpin)(SiMe3) compounds. Consecutive base-assisted transformations of HC(S)(B) (Si

GENERATION OF SULFUR YLIDES BY THE DESILYLATION OF α-TRIMETHYLSILYLBENZYL SULFONIUM SALTS

Padwa, Albert,Gasdaska, John R.

, p. 4147 - 4156 (2007/10/02)

The -sigmatropic rearrangement of sulfur ylides derived via the desilylation of several α-trimethylsilylbenzyl sulfonium salts has been studied.The initally formed ylide was found to rapidly equilibrate with the thermodynamically more stable ylide.In the absence of trapping reagents, a Sommelet-Hauser type rearrangement occurs.

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 17988-38-4