Welcome to LookChem.com Sign In|Join Free
  • or
C10H12O3S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1609274-93-2

Post Buying Request

1609274-93-2 Suppliers

Recommended suppliers

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

1609274-93-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1609274-93-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,9,2,7 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1609274-93:
(9*1)+(8*6)+(7*0)+(6*9)+(5*2)+(4*7)+(3*4)+(2*9)+(1*3)=182
182 % 10 = 2
So 1609274-93-2 is a valid CAS Registry Number.

1609274-93-2Upstream product

1609274-93-2Downstream Products

1609274-93-2Relevant academic research and scientific papers

Enantioselective oxidation of thioethers to sulfoxides by means of a structural template with chiral-at-metal ruthenium complexes

Li, Zheng-Zheng,Yao, Su-Yang,Ye, Bao-Hui

, p. 141 - 150 (2015/02/05)

Treatment of cis-[Ru(bpy)2Cl2]·2H2O or Δ/Λ-[Ru(bpy)2(py)2]2+ (bpy=2,2′-bipyridine, py=pyridine) with the prochiral thioether ligands 2-alkylthiobenzoic acid (HOS-R) produces the corresponding thioether complexes rac-[Ru(bpy)2(OS-R)](PF6) (R=Me (rac-1), iPr (rac-2), 2-benzylthiobenzonate (Bn) (rac-3)) and Δ/Λ-[Ru(bpy)2(OS-R)](PF6) (R=Me (Δ-1/Λ-1), iPr (Δ-2/Λ-2), Bn (Δ-3/Λ-3)) with retention of the configurations at chiral metal centers. In situ oxidation of the thioether complexes by metachloroperoxybenzoic acid provides the corresponding sulfoxide complexes rac-[Ru(bpy)2(OSO-R)](PF6) (OSO-R is 2-alkylsulfinylbenzonate, R=Me (rac-1a), iPr (rac-2a), Bn (rac-3a)), Δ-[Ru(bpy)2{(R)-OSO-R}](PF6) (R=Me (Δ-1a), iPr (Δ-2a), Bn (Δ-3a)), and Λ-[Ru(bpy)2{(S)-OSO-R}](PF6) (R=Me (Λ-1a), iPr (Λ-2a), Bn (Λ-3a)) in yields of 95% with 98% ee values. The absolute configurations at the metal centers and sulfur atoms were determined by means of X-ray crystallography. The results indicate that the configurations of the metal centers are retained and have the function of controlling sulfoxide chirality during the oxidation process. The Δ metal-centered configuration enantioselectively generates an R-configuration sulfoxide, and the Λ configuration enantioselectively forms an S-configuration sulfoxide in the course of the in situ oxidation reaction, thereby resulting in a predetermined chirality of the sulfoxide ligands. The predetermined chirality of sulfoxides (S)-HOSO-R and (R)-HOSO-R were obtained by the treatments of the corresponding sulfoxide complexes Δ-[Ru(bpy)2{(R )-OSO-R}](PF6) and Λ-[Ru(bpy)2{(S)-OSO-R}](PF6) with trifluoroacetic acid in yields of 90% with 83.5-92.9% ee values.

In situ generation of sulfoxides with predetermined chirality via a structural template with a chiral-at-metal ruthenium complex

Li, Zheng-Zheng,Yao, Su-Yang,Wu, Jin-Ji,Ye, Bao-Hui

supporting information, p. 5644 - 5647 (2014/05/20)

The reaction of Δ/Λ-[Ru(bpy)2(py)2] 2+ with a prochiral sulfide ligand, and then in situ oxidation, provide the corresponding Δ-[Ru(bpy)2{(R)-OSO-iPr}]+ and Λ-[Ru(bpy)2{(S)-OSO-iPr}]+ (OSO-iPr = 2-isopropylsulfonylbenzonate) enantiomers in a yield of 83% with 98% ee. The chiral sulfoxides were obtained by treatment of the sulfoxide complexes with TFA in a yield of 90% with 88-91% ee. the Partner Organisations 2014.

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 1609274-93-2