Welcome to LookChem.com Sign In|Join Free
  • or
C6H5CCCH(CH3)SC6H5 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

177615-85-9

Post Buying Request

177615-85-9 Suppliers

Recommended suppliers

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

177615-85-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 177615-85-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,6,1 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 177615-85:
(8*1)+(7*7)+(6*7)+(5*6)+(4*1)+(3*5)+(2*8)+(1*5)=169
169 % 10 = 9
So 177615-85-9 is a valid CAS Registry Number.

177615-85-9Downstream Products

177615-85-9Relevant academic research and scientific papers

The efficiency of the metal catalysts in the nucleophilic substitution of alcohols is dependent on the nucleophile and not on the electrophile

Biswas, Srijit,Samec, Joseph S. M.

, p. 974 - 981 (2013)

In this study, we investigate the effect of the electrophiles and the nucleophiles for eight catalysts in the catalytic SN1 type substitution of alcohols with different degree of activation by sulfur-, carbon-, oxygen-, and nitrogen-centered nucleophiles. The catalysts do not show any general variance in efficiency or selectivity with respect to the alcohols and follow the trend of alcohol reactivity. However, when it comes to the nucleophile, the eight catalysts show general and specific variances in the efficiency and selectivity to perform the desired substitution. Interestingly, the selectivity of the alcohols to produce the desired substitution products was found to be independent of the electrophilicity of the generated carbocations but highly dependent on the ease of formation of the cation. Catalysts based on iron(III), bismuth(III), and gold(III) show higher conversions for S-, C-, and N-centered nucleophiles, and BiIII was the most efficient catalyst in all combinations. Catalysts based on rhenium(I) or rhenium(VII), palladium(II), and lanthanum(III) were the most efficient in performing the nucleophilic substitution on the various alcohols with the O-centered nucleophiles. These catalysts generate the symmetrical ether as a by-product from the reactions of S-, C-, and N-centered nucleophiles as well, resulting in lower chemoselectivity. Who's the boss? In a comprehensive study of catalytic S N1 type direct substitution of alcohols, the catalysts do not show any general variance in efficiency or selectivity with respect to the alcohols but are highly variable with respect to the nucleophiles. The reactivity of the alcohols is independent of the electrophilicity of the generated carbocations but highly dependent on the ease of formation of the cation.

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 177615-85-9