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5-(3-methoxyphenyl)-2,3-dihydro-1H-inden-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

863479-23-6

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863479-23-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 863479-23-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,3,4,7 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 863479-23:
(8*8)+(7*6)+(6*3)+(5*4)+(4*7)+(3*9)+(2*2)+(1*3)=206
206 % 10 = 6
So 863479-23-6 is a valid CAS Registry Number.

863479-23-6Downstream Products

863479-23-6Relevant academic research and scientific papers

One-step highly selective borylation/Suzuki cross-coupling of two distinct aryl bromides in pure water

Xu, Shan Dong,Sun, Fang Zhou,Deng, Wei Hang,Hao, Han,Duan, Xin Hong

, p. 16464 - 16468 (2018)

A Na2PdCl4-catalysed B2(OH)4-mediated direct cross-coupling of two distinct aryl bromides in pure water is described. This one-step borylation/Suzuki method exhibits an outstanding cross-coupling selectivity and no tendency to produce homocoupling products, therefore leading to biaryls and heterobiaryls in moderate to good yields. Moreover, the reaction has high regio-selectivity and can be scaled-up. Using such a simple, economical and practical protocol, the unsymmetrical diarylation of 3,5-dibromopryidine is achieved.

6-Aryl-8H-indeno[1,2-d]thiazol-2-ylamines: A1 adenosine receptor agonist allosteric enhancers having improved potency

Chordia, Mahendra D.,Zigler, Molly,Murphree, Lauren J.,Figler, Heidi,Macdonald, Timothy L.,Olsson, Ray A.,Linden, Joel

, p. 5131 - 5139 (2007/10/03)

Allosteric enhancers (AEs) of the A1 adenosine receptor (A 1AR) have potential as drugs for treating neurological, cardiovascular, and renal diseases. This report describes the synthesis and evaluation of a series of 6-aryl-8H-indeno[1,2-d]thiazol-2-ylamines that exhibited AE activity at the A1AR. Palladium-mediated condensation of arylboronic acids with 5-bromoindan-1-one generated arylindanones 2a-aj for iodine-catalyzed condensation with thiourea, generating 2-aminothiazolium salts 3a-aj. Binding studies using membranes from cells stably expressing human A 1ARs, A2AARs, or A3ARs evaluated AE activity and receptor subtype selectivity. The EC50 of the AE activities of compounds 3m-o, 3x, and 3ae were 2.2, 1.5, 0.9, 1.0, and 3.0 μM, respectively, substantially lower than that of the well characterized 2-amino-3-aroylthiophene (PD 81,723), >10 μM. The new compounds also have substantially higher maximal AE activity. These compounds had no AE activity at the A2AAR and only minimal activity at the A3AR. 2005 American Chemical Society.

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