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N-(4-fluorophenyl)thioformamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

26060-32-2

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26060-32-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26060-32-2 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 26060-32:
(7*2)+(6*6)+(5*0)+(4*6)+(3*0)+(2*3)+(1*2)=82
82 % 10 = 2
So 26060-32-2 is a valid CAS Registry Number.

26060-32-2Downstream Products

26060-32-2Relevant academic research and scientific papers

Fe3O4@GlcA@Cu-MOF: A Magnetic Metal-Organic Framework as a Recoverable Catalyst for the Hydration of Nitriles and Reduction of Isothiocyanates, Isocyanates, and Isocyanides

Ghorbani-Choghamarani, Arash,Taherinia, Zahra

supporting information, p. 902 - 909 (2020/11/30)

A novel magnetic metal-organic framework (Fe3O4@GlcA@Cu-MOF) has been prepared and characterized by spectroscopic, microscopic, and magnetic techniques. This magnetically separable catalyst exhibited high catalytic activity for nitrile hydration and the ability to reduce isothiocyanates, isocyanates, and isocyanides with excellent activity and selectivity without any additional reducing agent.

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.

Synthesis of O-ethyl thioformate: A useful reagent for the thioformylation of amines

Borths, Christopher J.,Chan, Johann,Burke, Brenda J.,Larsen, Robert D.

experimental part, p. 3139 - 3142 (2010/03/24)

O-Ethyl thioformate has been synthesized from triethylorthoformate and hydrogen sulfide gas using a Bronstead acid catalyst. The product can be isolated as a neat liquid in 83% overall yield. Both the crude and purified thiolate can be used to thioformylate a variety of amines in good to excellent yields.

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