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3-(3-chlorophenyl)-1H-indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

252669-22-0

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252669-22-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 252669-22-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,2,6,6 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 252669-22:
(8*2)+(7*5)+(6*2)+(5*6)+(4*6)+(3*9)+(2*2)+(1*2)=150
150 % 10 = 0
So 252669-22-0 is a valid CAS Registry Number.

252669-22-0Downstream Products

252669-22-0Relevant articles and documents

Aerobic, Metal-Free, and Catalytic Dehydrogenative Coupling of Heterocycles: En Route to Hedgehog Signaling Pathway Inhibitors

Bering, Luis,Paulussen, Felix M.,Antonchick, Andrey P.

supporting information, p. 1978 - 1981 (2018/04/16)

The nitrosonium ion-catalyzed dehydrogenative coupling of heteroarenes under mild reaction conditions is reported. The developed method utilizes ambient molecular oxygen as a terminal oxidant, and only water is produced as byproduct. Dehydrogenative coupl

Palladium-catalyzed direct denitrogenative C-3-arylation of 1H-indoles with arylhydrazines using air as the oxidant

Chen, Yongxin,Guo, Shuaibo,Li, Kangning,Qu, Jinpeng,Yuan, Hua,Hua, Qiuru,Chen, Baohua

supporting information, p. 711 - 715 (2013/03/29)

A novel palladium-catalyzed approach to direct C-3-arylation of 1H-indoles with arylhydrazines using air as the oxidant via C-N bond cleavage has been developed. Various substituents are tolerated in this system in moderate to good yields. This reaction could also be compatible with a larger scale. Thus, this strategy using arylhydrazines as arylating reagents provides a powerful method for constructing substituted 3-aryl-1H-indoles. Copyright

"on water" direct and site-selective Pd-catalysed C-H arylation of (NH)-indoles

Joucla, Lionel,Batail, Nelly,Djakovitch, Laurent

supporting information; experimental part, p. 2929 - 2936 (2011/02/22)

This communication describes the development of a versatile catalytic system based on palladium(II) acetate/bis(diphenylphosphino)methane [Pd(OAc)2/dppm] that works "on water" giving site-selective C-H arylation of (NH)-indoles without protecting or directing groups. Remarkably, the control of regioselectivity was achieved by small changes in the "extra-catalytic" base/halide partners. These innovative methodologies allow a high-yielding access to both C2 and C3-arylindoles, as well as 2,3-diarylindoles, and display high chemo/regioselectivities and structural versatility with regard to either indole or aryl moieties. Copyright

Palladium-catalyzed direct C-3 arylations of indoles with an air-stable HASPO

Ackermann, Lutz,Barfü?er, Sebastian

experimental part, p. 808 - 812 (2009/07/18)

Efficient direct arylations of indoles occurred highly regioselectively at position C-3 with an in situ generated palladium complex derived from an air-stable HASPO, which enabled syntheses of diversely functionalized indoles, also with sterically hindere

Imidazolyl derivatives

-

, (2008/06/13)

The present invention is directed to imidazolyl derivatives of formula (I), wherein the variables are defined in the specification, which are useful as prenyl transferase inhibitors.

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