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2-Oxazolamine, 5-(4-chlorophenyl)-4,5-dihydro-N-phenyl- is a complex organic compound with the chemical formula C15H12ClNO. It is a derivative of oxazolamine, featuring a 4-chlorophenyl group attached to the 5-position of the oxazole ring, and a phenyl group connected to the nitrogen atom. 2-Oxazolamine, 5-(4-chlorophenyl)-4,5-dihydro-N-phenyl- is characterized by its unique molecular structure, which includes a five-membered oxazole ring fused to a dihydro structure. It is primarily used in the synthesis of various pharmaceuticals and agrochemicals due to its potential biological activity. The compound's specific properties, such as its reactivity and stability, make it a valuable intermediate in the development of new drugs and chemical products.

3920-06-7

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3920-06-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3920-06-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,2 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3920-06:
(6*3)+(5*9)+(4*2)+(3*0)+(2*0)+(1*6)=77
77 % 10 = 7
So 3920-06-7 is a valid CAS Registry Number.

3920-06-7Downstream Products

3920-06-7Relevant academic research and scientific papers

Cycloaddition of new N-unsubstituted azomethine ylides generated from N-(trimethylsilylmethyl)thioureas to electron-deficient olefins, acetylenes and aldehydes, synthetic equivalents of nonstabilized aminonitrile ylides

Tsuge, Otohiko,Hatta, Taizo,Tashiro, Hideki,Kakura, Yoshikazu,Maeda, Hironori,Kakehi, Akikazu

, p. 7723 - 7735 (2007/10/03)

The S-methylation of N-(trimethylsilylmethyl)thioureas and the subsequent desilylation of the silylmethyl group generates N-unsubstituted azomethine ylides having both methylthio and amino groups at the ylide carbon. These azomethine ylides undergo succes

N-(TRIMETHYLSILYLMETHYL)CARBODIIMIDES AND -KETENIMINE AS PRECURSORS OF IMINO- AND ALKYLIDENE-2-AZAALLYL ANIONS

Tsuge, Otohiko,Kanemasa, Shuji,Matsuda, Koyo

, p. 1827 - 1830 (2007/10/02)

The fluoride-induced desilylation of N-(trimethylsilylmethyl)carbodiimides and -ketenimine generates imino- and alkylidene-2-azaallyl anions which cycloadd to a variety of aldehydes giving regioisomeric 1,3-oxazolidines as cycloadducts.

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