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5-isopropyl-2-(p-tolyl)benzo[d]oxazole is a complex organic compound characterized by a benzoxazole ring structure. The benzoxazole ring is a fused ring system consisting of a benzene ring and an oxazole ring. In this specific compound, the benzene ring is substituted with an isopropyl group at the 5-position and a p-tolyl group (a tolyl group attached to the para position of the benzene ring) at the 2-position. This chemical is known for its potential applications in various fields, such as pharmaceuticals and materials science, due to its unique electronic and steric properties. The compound's structure provides a balance of lipophilicity and polarity, which can be beneficial for interactions with biological targets or as a component in advanced materials.

5998-46-9

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5998-46-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5998-46-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,9 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5998-46:
(6*5)+(5*9)+(4*9)+(3*8)+(2*4)+(1*6)=149
149 % 10 = 9
So 5998-46-9 is a valid CAS Registry Number.

5998-46-9Upstream product

5998-46-9Relevant academic research and scientific papers

Cu-Catalyzed Synthesis of Benzoxazole with Phenol and Cyclic Oxime

Wang, Zheng-Hai,Wang, Dong-Hui

, p. 782 - 785 (2022/01/20)

A Cu-catalyzed straightforward synthesis of benzoxazoles from free phenols and cyclic oxime esters is reported. The mild reaction conditions tolerate various electron-withdrawing and electron-donating functional groups on both substrates, affording benzoxazoles in moderate to good yields. With this protocol, large-scale syntheses of Ezutromid and Flunoxaprofe in one or two steps are demonstrated. A catalytic mechanism, which includes Cu-catalyzed amination via inner-sphere electron transfer and consequent annulation, is proposed.

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