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1224447-47-5

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1224447-47-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1224447-47-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,4,4,4 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1224447-47:
(9*1)+(8*2)+(7*2)+(6*4)+(5*4)+(4*4)+(3*7)+(2*4)+(1*7)=135
135 % 10 = 5
So 1224447-47-5 is a valid CAS Registry Number.

1224447-47-5Downstream Products

1224447-47-5Relevant articles and documents

Iridium-Catalyzed Aerobic Coupling of Salicylaldehydes with Alkynes: A Remarkable Switch of Oxacyclic Product

Yamane, Shintaro,Hinoue, Tomoaki,Usuki, Yoshinosuke,Itazaki, Masumi,Nakazawa, Hiroshi,Hayashi, Yoshihiro,Kawauchi, Susumu,Miura, Masahiro,Satoh, Tetsuya

supporting information, p. 7852 - 7855 (2018/05/08)

The iridium(III)/copper(II)-catalyzed dehydrogenative coupling of salicylaldehydes with internal alkynes proceeds efficiently under atmospheric oxygen through aldehyde C?H bond cleavage and decarbonylation. A variety of benzofuran derivatives can be synthesized by the environmentally benign procedure. DFT calculations suggest that this unique transformation involves the facile deinsertion of CO in the key metallacycle intermediate, which is in marked contrast to the corresponding rhodium(III) catalysis that leads to CO-retentive chromone derivatives.

A one-pot domino C-H, C-C activation in coumarins: A fast track to 2,3-diaryl benzo[b]furans

Khoobi, Mehdi,Molaverdi, Fatemeh,Jafarpour, Farnaz,Abbasnia, Masoumeh,Kubicki, Maciej,Shafiee, Abbas

supporting information, p. 11713 - 11716 (2015/07/15)

An approach to synthesize 2,3-diaryl benzo[b]furans using coumarins and aryl bromides is developed. This state-of-the-art strategy capitalizes on a palladium-catalyzed one-pot decarbonylative diarylation of coumarins, paving the way to achieve biologicall

Direct arylation of benzo[b]furan and other benzo-fused heterocycles

Dao-Huy, Toan,Haider, Maximilian,Glatz, Fabian,Schnürch, Michael,Mihovilovic, Marko D.

, p. 8119 - 8125 (2015/01/09)

The direct arylation of benzo[b]furan, benzo[b]thiophene, and indole has been studied by using aromatic bromides as the aryl source. The protocol employing common reagents and a Pd catalyst has led to the regioselective arylation of these heterocycles at the 2-position. A range of functional groups were tolerated, providing quick access to a variety of arylated benzo-fused heterocycles that would be accessible more elaborately using classical synthetic strategies. This is the first systematic study of the direct arylation of benzo[b]-furan.

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