Welcome to LookChem.com Sign In|Join Free
  • or
2-(4-nitrophenyl)-1,3-oxathiolan-5-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

37510-22-8

Post Buying Request

37510-22-8 Suppliers

Recommended suppliers

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

37510-22-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37510-22-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,5,1 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 37510-22:
(7*3)+(6*7)+(5*5)+(4*1)+(3*0)+(2*2)+(1*2)=98
98 % 10 = 8
So 37510-22-8 is a valid CAS Registry Number.

37510-22-8Downstream Products

37510-22-8Relevant academic research and scientific papers

Silica gel-promoted new one-pot procedure for the synthesis of 1,3-oxathiolan-5-one

Thakare, Manoj P.,Shaikh, Rahimullah,Tayade, Dipak

, p. 465 - 474 (2017)

A highly selective two-component silica gel-promoted synthesis of 1,3-oxathiolan-5-one derivatives in N,N-Dimethylformamide (DMF) is presented. The reaction was carried out using aromatic aldehyde and mercaptoacetic acid in the presence of silica gel in DMF with heating. The reactions were worked up by separating the silica gel and recovering the solid product after adding water in excellent yields without any chromatographic purification. Structures of the compounds were satisfactorily confirmed by 1H NMR and LCMS spectral analysis.

A facile and effective procedure for the synthesis of 4-thiazolidinone derivatives using Y(OTf)3 as catalyst

Luo, Juan,Zhong, Zijun,Ji, Hongfu,Chen, Jiayin,Zhao, Jun,Zhang, Furen

, p. 438 - 449 (2016/07/23)

ABSTRACT: A one-pot three-component reaction for the synthesis of 4-thiazolidinone derivatives has been established by reacting readily available and inexpensive starting materials of amines, aldehydes and thioglycolic acid using Y(OTf)3 (5 mol%) as catalyst in tetrahydrofuran. This method is very efficient due to low catalyst loading and mild reaction conditions and provides an efficient and promising synthetic strategy for the construction of the thiazolidinone skeleton.

Cobalt doped ZnS nanoparticles as a recyclable catalyst for solvent-free synthesis of heterocyclic privileged medicinal scaffolds under infrared irradiation

Dandia, Anshu,Parewa, Vijay,Gupta, Shyam L.,Rathore, Kuldeep S.

, p. 61 - 71 (2013/06/26)

This paper reports preparation and characterization of cobalt doped ZnS NPs and their catalytic application in the synthesis of heterocyclic privileged medicinal scaffolds involving pyrazolones (with excellent regioselectivity) and 1,3-oxathiolan-5-one frameworks under infrared irradiation. Nanoparticles have been prepared at room temperature by a wet chemical method. The heterogeneous catalysts were fully characterized by XRD, TEM, EDAX, ICP-AES and UV/Vis. Under infrared radiation (IR), the catalytic activity of Co doped ZnS NPs was about 40-fold higher under IR as compared to the conventional method. Nanocatalyst plays a dual role of catalyst as well as susceptor, and enhances the overall capacity to absorb IR in the reaction mixture. Doping by Co promotes the activity and selectivity of ZnS NPs as indicated by their high TOF value, providing the products with good to excellent yields. The surface acidity of NPs was measured by FTIR spectra of chemisorbed pyridine. The present method does not involve any hazardous organic solvent or catalyst. The introduction of nanocatalyst in an IR system offers promising features for the reaction response such as the shorter reaction time, simple work-up procedure, and purification of products by non-chromatographic methods. The catalyst was reused up to four runs without an appreciable loss of catalytic activity.

Molecular iodine in [bmim][BF4]: A highly efficient green catalytic system for one-pot synthesis of 1,3-oxathiolan-5-one

Dewan, Manika,Kumar, Ajeet,Saxena, Amit,De, Arnab,Mozumdar, Subho

experimental part, p. 6108 - 6110 (2011/01/04)

Aldehydes and mercaptoacetic acid are coupled in the presence of a catalytic amount of economical and non-toxic molecular iodine in [bmim][BF 4] ionic liquid under mild conditions to afford the corresponding 1,3-oxathiolan-5-one in excellent yields. Molecular iodine acts faster in ionic liquids when compared to conventional solvents such as DMSO, DMF, ethyl acetate, and acetonitrile. The recovered ionic liquids can be recycled in subsequent reactions with consistent activity.

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 37510-22-8