Welcome to LookChem.com Sign In|Join Free
  • or
Trithioboric acid triphenyl ester, also known as triphenyl trithioborate, is a chemical compound with the formula (C6H5)3B(SH)3. It is a colorless, crystalline solid that is soluble in organic solvents. trithioboric acid triphenyl ester is derived from trithioboric acid (B(SH)3) and phenol (C6H5OH), where the hydroxyl group of phenol is replaced by the trithioborate anion. Trithioboric acid triphenyl ester is used as a reagent in organic synthesis, particularly in the formation of carbon-sulfur bonds and as a ligand in coordination chemistry. It is also known for its potential applications in the synthesis of pharmaceuticals and agrochemicals. The compound is sensitive to air and moisture, and should be handled with care in a controlled environment.

1041-16-3

Post Buying Request

1041-16-3 Suppliers

Recommended suppliers

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

1041-16-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1041-16-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,4 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1041-16:
(6*1)+(5*0)+(4*4)+(3*1)+(2*1)+(1*6)=33
33 % 10 = 3
So 1041-16-3 is a valid CAS Registry Number.

1041-16-3Relevant academic research and scientific papers

Thermodynamic studies and hydride transfer reactions from a rhodium complex to BX3 compounds

Mock, Michael T.,Potter, Robert G.,Camaioni, Donald M.,Li, Jun,Dougherty, William G.,Kassel, W. Scott,Twamley, Brendan,DuBois, Daniel L.

experimental part, p. 14454 - 14465 (2010/02/16)

This study examines the use of transition-metal hydride complexes that can be generated by the heterolytic cleavage of H2 gas to form B-H bonds. Specifically, these studies are focused on providing a reliable and quantitative method for determining when hydride transfer from transition-metal hydrides to three-coordinate BX3 (X = OR, SPh, F, H; R = Ph, p-C 6H4OMe, C6F5, tBu, Si(Me)3) compounds will be favorable. This involves both experimental and theoretical determinations of hydride transfer abilities. Thermodynamic hydride donor abilities (ΔG°H-) were determined for HRh(dmpe)2 and HRh(depe)2, where dmpe ) 1,2-bis(dimethylphosphinoethane) and depe ) 1,2-bis(diethylphosphinoethane), on a previously established scale in acetonitrile. This hydride donor ability was used to determine the hydride donor ability of [HBEt3]- on this scale. Isodesmic reactions between [HBEt3]- and selected BX3 compounds to form BEt3 and [HBX3]- were examined computationally to determine their relative hydride affinities. The use of these scales of hydride donor abilities and hydride affinities for transition-metal hydrides and BX3 compounds is illustrated with a few selected reactions relevant to the regeneration of ammonia borane. Our findings indicate that it is possible to form B-H bonds from B-X bonds, and the extent to which BX3 compounds are reduced by transition-metal hydride complexes forming species containing multiple B-H bonds depends on the heterolytic B-X bond energy. An example is the reduction of B(SPh)3 using HRh(dmpe)2 in the presence of triethylamine to form Et 3N-BH3 in high yields.

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 1041-16-3