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methyl 6-isopropyl-1H-indole-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

213596-37-3

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213596-37-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 213596-37-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,3,5,9 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 213596-37:
(8*2)+(7*1)+(6*3)+(5*5)+(4*9)+(3*6)+(2*3)+(1*7)=133
133 % 10 = 3
So 213596-37-3 is a valid CAS Registry Number.

213596-37-3Downstream Products

213596-37-3Relevant academic research and scientific papers

Discovery of selective ATP-competitive eIF4A3 inhibitors

Ito, Masahiro,Iwatani, Misa,Kamada, Yusuke,Sogabe, Satoshi,Nakao, Shoichi,Tanaka, Toshio,Kawamoto, Tomohiro,Aparicio, Samuel,Nakanishi, Atsushi,Imaeda, Yasuhiro

, p. 2200 - 2209 (2017)

Eukaryotic initiation factor 4A3 (eIF4A3), an ATP-dependent RNA helicase, is a core component of exon junction complex (EJC). EJC has a variety of roles in RNA metabolism such as translation, surveillance, and localization of spliced RNA. It is worthwhile to identify selective eIF4A3 inhibitors with a view to investigating the functions of eIF4A3 and EJC further to clarify the roles of the ATPase and helicase activities in cells. Our chemical optimization of hit compound 2 culminated in the discovery of ATP-competitive eIF4A3 inhibitor 18 with submicromolar ATPase inhibitory activity and excellent selectivity over other helicases. Hence, compound 18 could be a valuable chemical probe to elucidate the detailed functions of eIF4A3 and EJC.

Intramolecular C-H amination reactions: Exploitation of the Rh 2(II)-catalyzed decomposition of azidoacrylates

Stokes, Benjamin J.,Dong, Huijun,Leslie, Brooke E.,Pumphrey, Ashley L.,Driver, Tom G.

, p. 7500 - 7501 (2008/02/09)

Rhodium(II) perfluorobutyrate-mediated decomposition of vinyl azides provides a new, mild entry into Rh2(II) nitrenoid chemistry. This methodology allows rapid access to a variety of complex, functionalized N-heterocycles in two steps from commercially available starting materials. Copyright

Stille and suzuki cross coupling reactions of o-nitrophenyl triflates: A versatile route to a variety of heterocycles

Holzapfel, Cedric W.,Dwyer, Catherine

, p. 1513 - 1518 (2007/10/03)

The cross coupling reactions of selected o-nitrophenyl triflates with arylstannane and arylboron substrates are reported. The resultant 2-nitrobiphenyls provide ready access to a variety of substituted heterocycles.

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