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2-methyl-1-phenyl-2-thiocyanatopropan-1-one is a complex organic chemical compound with the molecular formula C12H13KNS. It is a derivative of acetophenone, featuring a methyl group (CH3), a phenyl ring (C6H5), and a thiocyanate group (SCN) attached to the carbonyl (C=O) functional group. 2-methyl-1-phenyl-2-thiocyanatopropan-1-one is characterized by its unique structure, which combines the properties of a ketone with those of a thiocyanate. It is typically synthesized through the reaction of acetophenone with a thiocyanate source, such as potassium thiocyanate (KSCN). The compound may have potential applications in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals due to its reactivity and the presence of multiple functional groups. However, it is important to note that the specific uses and properties of 2-methyl-1-phenyl-2-thiocyanatopropan-1-one would require further investigation and characterization.

3034-29-5

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3034-29-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3034-29-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,3 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3034-29:
(6*3)+(5*0)+(4*3)+(3*4)+(2*2)+(1*9)=55
55 % 10 = 5
So 3034-29-5 is a valid CAS Registry Number.

3034-29-5Downstream Products

3034-29-5Relevant academic research and scientific papers

Redox Active Sodium Iodide/Recyclable Heterogeneous Solid Acid: An Efficient Dual Catalytic System for Electrochemically Oxidative α-C?H Thiocyanation and Sulfenylation of Ketones

Liang, Sen,Zeng, Cheng-Chu,Tian, Hong-Yu,Sun, Bao-Guo,Luo, Xu-Gang,Ren, Fa-Zheng

, p. 1444 - 1452 (2017/12/18)

An efficient electrochemically oxidative α-C?H thiocyanation and sulfenylation of ketones has been developed in a simple undivided cell under constant current condition.?The electrochemistry performs using NaI as the redox catalyst and heterogeneous solid salt Amberlyst-15(H) (A-15(H)) as proton catalyst?without the addition of external conductive salts. The protocol proved to be practical since the solid salt could be reused in up to five consecutive gram-scale runs without significant decrease in efficiency. Control experiments and cyclic voltammetry analysis disclose that the reaction proceeds likely via a cascade α-halogenation and subsequent thiocyanation or sulfenylation. (Figure presented.).

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