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N,N-diallyl-(2-bromophenyl)amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

159766-59-3

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159766-59-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 159766-59-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,7,6 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 159766-59:
(8*1)+(7*5)+(6*9)+(5*7)+(4*6)+(3*6)+(2*5)+(1*9)=193
193 % 10 = 3
So 159766-59-3 is a valid CAS Registry Number.

159766-59-3Relevant academic research and scientific papers

Borane Catalyzed Redox Isomerization of 2-Amino Chalcones: Hydride Abstraction or Hydride Migration?

Zhou, Rundong,Paradies, Jan

supporting information, p. 6334 - 6339 (2021/09/25)

The borane catalyzed redox isomerization of 2-amino chalcones was developed. The tetrahydroquinolines are obtained in high yield as a mixture of cis/trans diastereomers in a ratio of 2 : 1 to >95 : 5. The reaction mechanism is investigated by mechanistic,

Highly selective N-allylation of anilines under microwave irradiation

Liu, Meiyu,Wang, Xie,Sun, Xiaoliang,He, Wei

, p. 2711 - 2714 (2014/05/06)

An easy and rapid procedure for the preparation of a variety of mono- and bis-allylated anilines via the reaction of allyl bromide with a wide range of anilines under microwave irradiation is described. This approach allows use of mild conditions and short reaction times to give high selectivities and excellent yields.

From PtCl2- and acid-catalyzed to uncatalyzed cycloisomerization of 2-propargyl anilines: Access to functionalized indoles

Cariou, Kevin,Ronan, Baptiste,Mignani, Serge,Fensterbank, Louis,Malacria, Max

, p. 1881 - 1884 (2008/03/12)

(Chemical Equation Presented) On the move: PtCl2-catalyzed electrophilic activation of an alkyne moiety triggers a heterocyclization accompanied by migrations of both an allyl group and an acetate group to produce an indole (see scheme). Variat

Synthesis of polysubstituted indoles and indolines by means of zirconocene-stabilized benzyne complexes

Tidwell, Jeffrey H.,Buchwald, Stephen L.

, p. 11797 - 11810 (2007/10/02)

The development of a new method for the regiospecific synthesis of polysubstituted indoles and indolines is reported. The key steps involve the generation of zirconocene-stabilized benzyne complexes and subsequent intramolecular olefin insertion reactions to provide tricyclic indoline zirconacycles. The zirconacyclic intermediates were cleaved with iodine to yield diiodo indolines, which were converted to a wide variety of indole and indoline products, such as analogs of tryptamine, serotonin, tryptophan, and the pharmacophore of CC-1065.

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