Welcome to LookChem.com Sign In|Join Free
  • or
Benzenesulfonothioic acid, 4-methyl-, S-(2-phenylethyl) ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53603-17-1

Post Buying Request

53603-17-1 Suppliers

Recommended suppliers

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

53603-17-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53603-17-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,0 and 3 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 53603-17:
(7*5)+(6*3)+(5*6)+(4*0)+(3*3)+(2*1)+(1*7)=101
101 % 10 = 1
So 53603-17-1 is a valid CAS Registry Number.

53603-17-1Relevant academic research and scientific papers

FACILE AND EFFICIENT SYNTHESIS OF ALKYL THIOTOSYLATES USING ANION EXCHANGE RESIN

Takano, Seiichi,Hiroya, Kou,Ogasawara, Kunio

, p. 255 - 256 (1983)

Facile and efficient synthesis of alkyl thiotosylates (1a-h) has been developed using anion exchange resin.

Perfluoroalkylation of Thiosulfonates: Synthesis of Perfluoroalkyl Sulfides

Luo, Ziwei,Yang, Xinkan,Tsui, Gavin Chit

supporting information, p. 6155 - 6159 (2020/07/30)

A practical synthesis of perfluoroalkyl sulfides is described. The method employs stable and readily accessible thiosulfonates as new electrophiles with commercial nucleophilic perfluoroalkylating reagents. The mild reaction conditions allow access to a wide variety of both aryl- and alkyl-substituted perfluoroalkyl sulfides amenable to pharmaceutical development. Furthermore, the reaction operation is straightforward, odorless, does not produce toxic wastes, and, therefore should appeal to practitioners in industrial-scale productions.

Metal-Free Synthesis of Thiosulfonates via Insertion of Sulfur Dioxide

Li, Guoqing,Gan, Ziyu,Kong, Kexin,Dou, Xiaomeng,Yang, Daoshan

supporting information, p. 1808 - 1814 (2019/03/28)

A simple and catalyst-free strategy was developed for the synthesis of unsymmetrical thiosulfonates using readily available DABCO?(SO2)2 as a solid and bench-stable sulfur dioxide surrogate. The corresponding thiosulfonates were obtained through a radical pathway with good functional group tolerance. This strategy offers a promising synthesis method for the construction of diverse and useful thiosulfonates in the field of synthetic and pharmaceutical chemistry and extends the number of still limited sulfur dioxide fixation strategies. (Figure presented.).

Method for synthesizing thiosulfonate compounds on the basis of strategy of SO2 insertion

-

Paragraph 0123; 0124; 0125; 0126; 0127; 0128, (2019/04/26)

The invention relates to a method for synthesizing thiosulfonate compounds on the basis of strategy of SO2 insertion. The method includes: performing a reaction in the presence of nitrogen gas and atcertain temperature to prepare the thiosulfonate compoun

A FACILE SYNTHESIS OF UNSYMMETRICAL THIOSULFONATES VIA SULFONYLATION OF MERCAPTANS

Ranasinghe, M. G.,Fuchs, P. L.

, p. 227 - 232 (2007/10/02)

The reaction of p-toluenesulfonyl bromide with mercaptans provides a convenient procedure for the synthesis of unsymmetrical thiolsulfonates.

New Synthetic Methods, 9. - S-Alkyl 4-Methylbenzenethiosulfonates, Excellent Reagents for α-Thiolation of Cyclic Ketones

Scholz, Dieter

, p. 259 - 263 (2007/10/02)

S-Alkyl 4-methylbenzenethiosulfonates, easily prepared by alkylation of commercially available potassium 4-methylbenzenethiosulfonate in dry dimethylformamide, thiolate enolates of cyclic ketones in α position in high yield.

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 53603-17-1