Welcome to LookChem.com Sign In|Join Free
  • or
N-(4-methylphenyl)thioformamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

26060-31-1

Post Buying Request

26060-31-1 Suppliers

Recommended suppliers

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

26060-31-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26060-31-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,0,6 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 26060-31:
(7*2)+(6*6)+(5*0)+(4*6)+(3*0)+(2*3)+(1*1)=81
81 % 10 = 1
So 26060-31-1 is a valid CAS Registry Number.

26060-31-1Relevant academic research and scientific papers

Compound comprising urea and thiourea structures and synthesis method and application of compound

-

Paragraph 0064-0065, (2019/08/07)

The invention relates to an organic small molecular compound comprising urea and thiourea structures in a formula I and a synthesis method and application of the compound. According to in-vitro antitumor activity tests, the compound has high antitumor act

Chemoselective reduction of isothiocyanates to thioformamides mediated by the Schwartz reagent

De La Vega-Hernández, Karen,Senatore, Raffaele,Miele, Margherita,Urban, Ernst,Holzer, Wolfgang,Pace, Vittorio

supporting information, p. 1970 - 1978 (2019/02/20)

Thioformamides are easily prepared-under full chemocontrol-through the partial reduction of isothiocyanates with the in situ generated Schwartz reagent. The high electrophilicity of the starting materials enables the straightforward addition of the hydride ion, thus constituting a reliable and high-yielding method for obtaining variously functionalized thioformamides. Sensitive chemical groups to the reduction conditions such as nitro, ester, alkene, azo, azide and keto groups do not interfere with the chemoselectivity of the process. Moreover, the stereochemical information embodied in the starting material is fully retained in the final products. The synthetic potential of the selected thioformamide template is also briefly discussed.

Direct Conversion of Formanilides into Thioformanilides Using Solubilized Phosphorus Pentasulphide

Rao, C. Someswara,Murty, V. S. N.,Tattu, P. K.

, p. 1083 - 1084 (2007/10/02)

Direct conversion of formanilides into thioformanilides, not reported so far, has now been achieved in good to excellent yields using solubilized phosphorus pentasulphide of controlled reactivity.

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 26060-31-1