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4H-[1]Benzopyrano[3,4-d]oxazol-4-one, 2-(4-chlorophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63153-37-7

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63153-37-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63153-37-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,1,5 and 3 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 63153-37:
(7*6)+(6*3)+(5*1)+(4*5)+(3*3)+(2*3)+(1*7)=107
107 % 10 = 7
So 63153-37-7 is a valid CAS Registry Number.

63153-37-7Upstream product

63153-37-7Downstream Products

63153-37-7Relevant academic research and scientific papers

Synthesis of fused oxazole-containing coumarin derivatives via oxidative cross coupling reaction using a combination of CuCl2 and TBHP

Belal, Md.,Khan, Abu T.

, p. 18891 - 18894 (2016)

Various fused oxazoles containing coumarin derivatives were synthesized via an oxidative cross coupling reaction by employing 20 mol% CuCl2 as the catalyst and TBHP as an oxidant. The reaction proceeds through functionalization of a C-H bond by

Synthesis and reactions of 3-aroyl derivatives of 4-hydroxy-2-quinolones and 4-hydroxycoumarin

Kappe, Thomas,Schnell, Barbara

, p. 663 - 670 (2007/10/03)

3-Aroyl-4-hydroxy-2-quinolones 4 and 11 can be synthesized starting with 1 or 9 via Fries rearrangement of the corresponding esters 3 and 10, catalyzed by potassium cyanide and 18-crown-6. A one pot procedure is presented in which the esters do not need to be isolated. Reduction of the aryl ketones 4 and 11 with zinc dust leads to the benzyl derivatives 5 and 12. Reaction of the aryl ketones 4 and 11 with hydroxylamine and subsequent heating of the crude product leads via thermal Beckmann rearrangement and dehydration to oxazoloquinolones 7 and 14. 2-Aroyloxypyrido[1,2-a]pyrimidin-4-ones 17 and 20 could not be converted to the corresponding ketones by Fries rearrangement.

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