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Benzeneacetamide, N-(2,6-dimethylphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18109-37-0

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18109-37-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18109-37-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,0 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 18109-37:
(7*1)+(6*8)+(5*1)+(4*0)+(3*9)+(2*3)+(1*7)=100
100 % 10 = 0
So 18109-37-0 is a valid CAS Registry Number.

18109-37-0Relevant academic research and scientific papers

Chemoselective Reductive Deoxygenation and Reduction of α-Keto Amides by using a Palladium Catalyst

Mamillapalli, N. Chary,Sekar, Govindasamy

, p. 3273 - 3283 (2015)

A palladium catalyst is used to synthesize 2,N-diphenylacetamides and α-hydroxy amides from readily available α-keto amides by chemoselective reductive deoxygenation and chemoselective reduction using polymethylhydrosiloxane (PMHS). This methodology has t

Clean, reusable and low cost heterogeneous catalyst for amide synthesis

Comerford, James W.,Clark, James H.,MacQuarrie, Duncan J.,Breeden, Simon W.

, p. 2562 - 2564 (2009)

We have developed a heterogeneous silica catalyst that can effectively catalyse amide synthesis from acid and amine, without production of toxic by-products and with the advantage of being readily available, low cost, environmentally benign and reusable. The Royal Society of Chemistry 2009.

Oxidative C-H homodimerization of phenylacetamides

Pintori, Didier G.,Greaney, Michael F.

supporting information; experimental part, p. 5713 - 5715 (2011/12/04)

A range of secondary and tertiary phenylacetamides undergo oxidative homodimerization to afford biaryls. The reaction proceeds under palladium catalysis in the presence of a copper cocatalyst and oxygen and is most effective for electron-rich substrates.

ANALIDI AD ATTIVITA ANALGESICA ED ANTIPIRETICA

Mule, A.,Pirisino, G.,Piu, L.,Satta, M.,Manca, P.,Peana, A.

, p. 25 - 33 (2007/10/02)

Several trimethylcyclopentyl and trimethylcyclopentenyl acetanilides, mono- and di-substituted on the aromatic nucleus as well as the corresponding acyl derivatives from aniline it self and corresponding phenylacetanilides, were prepared and tested as analgesics and antipyretics.Several compounds exhibit considerable activity in some cases superior to that of acetanilide.

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