Welcome to LookChem.com Sign In|Join Free
  • or
(R)-phenyl(1-phenylethyl)selane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

819850-07-2

Post Buying Request

819850-07-2 Suppliers

Recommended suppliers

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

819850-07-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 819850-07-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,9,8,5 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 819850-07:
(8*8)+(7*1)+(6*9)+(5*8)+(4*5)+(3*0)+(2*0)+(1*7)=192
192 % 10 = 2
So 819850-07-2 is a valid CAS Registry Number.

819850-07-2Downstream Products

819850-07-2Relevant academic research and scientific papers

Transition metal-free coupling reactions of benzylic trimethylammonium salts with di(hetero)aryl disulfides and diselenides

Li, Fuhai,Wang, Dan,Chen, Hongyi,He, Ze,Zhou, Lihong,Zeng, Qingle

, p. 13029 - 13032 (2020/11/07)

A new protocol was developed to synthesize (enantioenriched) thioethers and selenoethers from (chiral) benzylic trimethylammonium salts and di(hetero)aryl disulfides or diselenides. These syntheses were promoted by the presence of weak base and did not require the use of any transition metal, and resulted in the target products with good to excellent yields (72-94%). Using quaternary ammonium salts synthesized from enantiomerically enriched amines led to highly enantiopure benzylic thioethers and selenoethers (94-99% ee) with configurations reversed from those of their enantioenriched quaternary ammonium salts. This journal is

Chemoenzymatic approaches to obtain chiral-centered selenium compounds

Brondani, Patricia B.,Guilmoto, Nathalie M. A. F.,Andrade, Leandro H.,Dudek, Hanna M.,Fraaije, Marco W.

, p. 10431 - 10436,6 (2012/12/12)

The synthesis of chiral-centered selenium compounds is presented. Enantioselective oxidations of these organoselenium compounds were performed using a wide range of biocatalysts, including Baeyer-Villiger monooxygenases, oxidoreductases-containing Aspergillus terreus and lipase (Cal-B) in the presence of oxidants. Finally, efficient synthesis of enantiopure organoselenium compounds using a kinetic resolution approach mediated by Cal-B was achieved.

Chemoenzymatic approaches to obtain chiral-centered selenium compounds

Brondani, Patrícia B.,Guilmoto, Nathalie M.A.F.,Dudek, Hanna M.,Fraaije, Marco W.,Andrade, Leandro H.

, p. 10431 - 10436 (2013/01/15)

The synthesis of chiral-centered selenium compounds is presented. Enantioselective oxidations of these organoselenium compounds were performed using a wide range of biocatalysts, including Baeyer-Villiger monooxygenases, oxidoreductases-containing Aspergillus terreus and lipase (Cal-B) in the presence of oxidants. Finally, efficient synthesis of enantiopure organoselenium compounds using a kinetic resolution approach mediated by Cal-B was achieved.

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 819850-07-2