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36756-13-5

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36756-13-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36756-13-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,7,5 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 36756-13:
(7*3)+(6*6)+(5*7)+(4*5)+(3*6)+(2*1)+(1*3)=135
135 % 10 = 5
So 36756-13-5 is a valid CAS Registry Number.

36756-13-5Downstream Products

36756-13-5Relevant articles and documents

Utilizing the chemiluminescence of 2-substituted-4,5-di(2-furyl)-1H- imidazole-H2O2-Cu2+ system for the determination of Cu2+

Zhang, Yihua,Kang, Jing,Zheng, Yumin,Han, Lu,Tang, Jieli,Wang, Shuaijun

, p. 376 - 382 (2011)

In the paper, 2,4,5-tri(2-furyl)-1H-imidazole (TFI) and 2-phenyl-4,5-di(2-furyl)-1H-imidazole (PDFI), were chosen to investigate chemiluminescence (CL) properties of 2-substituted-4,5-di(2-furyl)-1H- imidazoles. The directly oxidized CL of analytes by Hs

TMSOTf-catalyzed synthesis of trisubstituted imidazoles using hexamethyldisilazane as a nitrogen source under neat and microwave irradiation conditions

Asressu, Kesatebrhan Haile,Chan, Chieh-Kai,Wang, Cheng-Chung

, p. 28061 - 28071 (2021/09/15)

In the process of drug discovery and development, an efficient and expedient synthetic method for imidazole-based small molecules from commercially available and cheap starting materials has great significance. Herein, we developed a TMSOTf-catalyzed synthesis of trisubstituted imidazoles through the reaction of 1,2-diketones and aldehydes using hexamethyldisilazane as a nitrogen source under microwave heating and solvent-free conditions. The chemical structures of representative trisubstituted imidazoles were confirmed using X-ray single-crystal diffraction analysis. This synthetic method has several advantages including the involvement of mild Lewis acid, being metal- and additive-free, wide substrate scope with good to excellent yields and short reaction time. Furthermore, we demonstrate the application of the methodology in the synthesis of biologically active imidazole-based drugs.

CO2-assisted synthesis of non-symmetric α-diketones directly from aldehydes: Via C-C bond formation

Hirapara, Pradipbhai,Riemer, Daniel,Hazra, Nabanita,Gajera, Jignesh,Finger, Markus,Das, Shoubhik

supporting information, p. 5356 - 5360 (2017/11/22)

CO2-assisted various symmetric and non-symmetric α-diketones have been synthesized directly from the corresponding aldehydes using transition metal-free catalysts. This method can even be applied to synthesize pharmaceuticals directly from aldehydes. The crucial role of CO2 has been investigated in detail and the mechanism is proposed on the basis of experiments and DFT calculations.

Lewis acid catalyst free synthesis of substituted imidazoles in 2,2,2-trifluoroethanol

Khaksar, Samad,Alipour, Mandana

, p. 395 - 398 (2013/05/21)

A simple, inexpensive, environmentally friendly, and efficient route for the synthesis of highly substituted imidazoles by the condensation of 1,2-dicarbonyl compounds, aldehydes, and ammonium acetate using 2,2,2-trifluoroethanol as a solvent is described. The solvent can be readily separated from reaction products and recovered in excellent purity for direct reuse.

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